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dbVar

Database of genomic structural variation

nsv6534312

Organism: Homo sapiens

Study:nstd223 (Sedlazeck 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:7,638

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

Submitted genomic12,517,643-12,525,280

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6534312	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	12,517,643	12,525,280
nsv6534312	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	12,628,457	12,636,094

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18197346	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18197346	Submitted genomic		NC_000019.10:g.125 17643_12525280dup	GRCh38 (hg38)		NC_000019.10	Chr19	12,517,643	12,525,280
nssv18197346	Remapped	Perfect	NC_000019.9:g.1262 8457_12636094dup	GRCh37.p13	First Pass	NC_000019.9	Chr19	12,628,457	12,636,094

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv18197346	<0.001	2	39224

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