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dbVar

Database of genomic structural variation

nsv4748106

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:255

Publication(s):Quan et al. 2021

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: 141 SVs from 33 studies. See in: genome view

Remapped(Score: Perfect):33,081,869-33,082,123

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4748106	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	33,081,869	33,082,123
nsv4748106	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	33,572,775	33,573,029

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16265789	deletion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16265789	Remapped	Perfect	NC_000019.10:g.330 81869_33082123del	GRCh38.p12	First Pass	NC_000019.10	Chr19	33,081,869	33,082,123
nssv16265789	Submitted genomic		NC_000019.9:g.3357 2775_33573029del	GRCh37 (hg19)		NC_000019.9	Chr19	33,572,775	33,573,029

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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