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dbVar

Database of genomic structural variation

nsv4651153

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:5
Validation:Not tested
Clinical Assertions: No
Region Size:34,600

Description:nsv4043740 from gnomAD Structural Variants. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 116 SVs from 32 studies. See in: genome view

Remapped(Score: Good):60,001-94,600

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4651153	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	60,001	94,600
nsv4651153	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	60,000	94,600

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16157118	copy number variation	Curated	Curated
nssv16172671	copy number variation	Curated	Curated
nssv16172932	copy number variation	Curated	Curated
nssv16177503	copy number variation	Curated	Curated
nssv16179660	copy number variation	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16157118	Remapped	Good	GRCh38.p12	First Pass	NC_000019.10	Chr19	60,001	94,600
nssv16172671	Remapped	Good	GRCh38.p12	First Pass	NC_000019.10	Chr19	60,001	94,600
nssv16172932	Remapped	Good	GRCh38.p12	First Pass	NC_000019.10	Chr19	60,001	94,600
nssv16177503	Remapped	Good	GRCh38.p12	First Pass	NC_000019.10	Chr19	60,001	94,600
nssv16179660	Remapped	Good	GRCh38.p12	First Pass	NC_000019.10	Chr19	60,001	94,600
nssv16157118	Submitted genomic		GRCh37 (hg19)		NC_000019.9	Chr19	60,000	94,600
nssv16172671	Submitted genomic		GRCh37 (hg19)		NC_000019.9	Chr19	60,000	94,600
nssv16172932	Submitted genomic		GRCh37 (hg19)		NC_000019.9	Chr19	60,000	94,600
nssv16177503	Submitted genomic		GRCh37 (hg19)		NC_000019.9	Chr19	60,000	94,600
nssv16179660	Submitted genomic		GRCh37 (hg19)		NC_000019.9	Chr19	60,000	94,600

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16157118	0.288	3128	10847
nssv16172671	0.078	848	10847
nssv16172932	0.199	2155	10847
nssv16177503	0.012	130	10847
nssv16179660	0.419	4544	10847

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