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dbVar

Database of genomic structural variation

nsv4854880

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:378,262

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: 2906 SVs from 96 studies. See in: genome view

Remapped(Score: Perfect):928,895-1,307,158

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4854880	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	928,896 (-1)	1,307,157 (-1, +1)
nsv4854880	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	928,896 (-1)	1,307,156 (-1, +1)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16390484	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16390484	Remapped	Perfect	NC_000019.10:g.(92 8895_?)_(1307156_1 307158)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	928,896 (-1)	1,307,157 (-1, +1)
nssv16390484	Submitted genomic		NC_000019.9:g.(928 895_?)_(1307155_13 07157)dup	GRCh37 (hg19)		NC_000019.9	Chr19	928,896 (-1)	1,307,156 (-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)
nssv16390484	<0.001	1	16834

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