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dbVar

Database of genomic structural variation

nsv5662832

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert 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: 84 SVs from 21 studies. See in: genome view

Submitted genomic70,122,187-70,122,187

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5662832	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	70,122,187	70,122,187
nsv5662832	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	69,968,293	69,968,293

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17075828	insertion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17075828	Submitted genomic		NC_000011.10:g.701 22187_70122188ins2 10	GRCh38 (hg38)		NC_000011.10	Chr11	70,122,187	70,122,187
nssv17075828	Remapped	Perfect	NC_000011.9:g.6996 8293_69968294ins21 0	GRCh37.p13	First Pass	NC_000011.9	Chr11	69,968,293	69,968,293

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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