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dbVar

Database of genomic structural variation

nsv4713987

Organism: Homo sapiens

Study:nstd195 (Mwapagha et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):Mwapagha 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: 95 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):21,584,620-21,584,620

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4713987	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	21,584,620	21,584,620
nsv4713987	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	21,626,112	21,626,112

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv16239636	insertion	M478	Sequencing	Paired-end mapping	1	4,557

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16239636	Remapped	Perfect	NC_000003.12:g.215 84620_21584621ins3 09	GRCh38.p12	First Pass	NC_000003.12	Chr3	21,584,620	21,584,620
nssv16239636	Submitted genomic		NC_000003.11:g.216 26112_21626113ins3 09	GRCh37 (hg19)		NC_000003.11	Chr3	21,626,112	21,626,112

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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