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dbVar

Database of genomic structural variation

nsv6526918

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:515

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: 111 SVs from 30 studies. See in: genome view

Submitted genomic45,176,767-45,177,281

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6526918	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	45,176,767	45,177,281
nsv6526918	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	45,680,025	45,680,539

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18198870	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18198870	Submitted genomic		NC_000019.10:g.451 76767_45177281dup	GRCh38 (hg38)		NC_000019.10	Chr19	45,176,767	45,177,281
nssv18198870	Remapped	Perfect	NC_000019.9:g.4568 0025_45680539dup	GRCh37.p13	First Pass	NC_000019.9	Chr19	45,680,025	45,680,539

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)
nssv18198870	<0.001	9	37594

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