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dbVar

Database of genomic structural variation

nsv6535570

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:4,200

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: 1070 SVs from 68 studies. See in: genome view

Submitted genomic46,500,401-46,504,600

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6535570	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	46,500,401	46,504,600
nsv6535570	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	44,577,767	44,581,966

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18183881	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18183881	Submitted genomic		NC_000017.11:g.465 00401_46504600dup	GRCh38 (hg38)		NC_000017.11	Chr17	46,500,401	46,504,600
nssv18183881	Remapped	Perfect	NC_000017.10:g.445 77767_44581966dup	GRCh37.p13	First Pass	NC_000017.10	Chr17	44,577,767	44,581,966

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)
nssv18183881	0.301	10455	34696

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