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dbVar

Database of genomic structural variation

nsv6333556

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:3,030,800

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: 8714 SVs from 124 studies. See in: genome view

Submitted genomic24,890,501-27,921,300

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6333556	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	24,890,501	27,921,300
nsv6333556	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	25,216,992	28,247,811

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18202822	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18202822	Submitted genomic		NC_000001.11:g.248 90501_27921300dup	GRCh38 (hg38)		NC_000001.11	Chr1	24,890,501	27,921,300
nssv18202822	Remapped	Good	NC_000001.10:g.252 16992_28247811dup	GRCh37.p13	First Pass	NC_000001.10	Chr1	25,216,992	28,247,811

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)
nssv18202822	<0.001	4	20128

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