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dbVar

Database of genomic structural variation

nsv4973597

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:31,146

Publication(s):Abel et al. 2020

Links to Other Resources

Overlapping Genes

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: 119 SVs from 27 studies. See in: genome view

Submitted genomic45,298,388-45,329,645

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4973597	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	45,298,451 (-63)	45,329,596 (-3, +49)
nsv4973597	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	45,793,899 (-63)	45,825,044 (-3, +49)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16534279	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16534279	Submitted genomic		NC_000010.11:g.(45 298388_?)_(4532959 3_45329645)dup	GRCh38 (hg38)		NC_000010.11	Chr10	45,298,451 (-63)	45,329,596 (-3, +49)
nssv16534279	Remapped	Perfect	NC_000010.10:g.(45 793836_?)_(4582504 1_45825093)dup	GRCh37.p13	First Pass	NC_000010.10	Chr10	45,793,899 (-63)	45,825,044 (-3, +49)

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)
nssv16534279	<0.001	1	29246

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