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dbVar

Database of genomic structural variation

nsv4865133

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:502,805

Publication(s):Abel et al. 2020

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: 1782 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):35,722,805-36,225,611

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4865133	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	35,722,806 (-1)	36,225,610 (-1, +1)
nsv4865133	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	36,213,708 (-1)	36,716,512 (-1, +1)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16390266	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16390266	Remapped	Perfect	NC_000019.10:g.(35 722805_?)_(3622560 9_36225611)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	35,722,806 (-1)	36,225,610 (-1, +1)
nssv16390266	Submitted genomic		NC_000019.9:g.(362 13707_?)_(36716511 _36716513)dup	GRCh37 (hg19)		NC_000019.9	Chr19	36,213,708 (-1)	36,716,512 (-1, +1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16390266	<0.001	1	16834

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