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dbVar

Database of genomic structural variation

nsv6510019

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:576,869

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: 1370 SVs from 72 studies. See in: genome view

Submitted genomic95,535,227-96,112,095

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6510019	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	95,535,227	96,112,095
nsv6510019	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	96,001,564	96,578,432

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18190568	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18190568	Submitted genomic		NC_000014.9:g.9553 5227_96112095dup	GRCh38 (hg38)		NC_000014.9	Chr14	95,535,227	96,112,095
nssv18190568	Remapped	Perfect	NC_000014.8:g.9600 1564_96578432dup	GRCh37.p13	First Pass	NC_000014.8	Chr14	96,001,564	96,578,432

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)
nssv18190568	<0.001	1	39296

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