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dbVar

Database of genomic structural variation

nsv6462445

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:424,666

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: 1171 SVs from 79 studies. See in: genome view

Submitted genomic83,636,250-84,060,915

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6462445	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	83,636,250	84,060,915
nsv6462445	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	84,030,029	84,454,694

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18182836	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18182836	Submitted genomic		NC_000012.12:g.836 36250_84060915dup	GRCh38 (hg38)		NC_000012.12	Chr12	83,636,250	84,060,915
nssv18182836	Remapped	Perfect	NC_000012.11:g.840 30029_84454694dup	GRCh37.p13	First Pass	NC_000012.11	Chr12	84,030,029	84,454,694

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)
nssv18182836	<0.001	3	39298

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