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dbVar

Database of genomic structural variation

nsv5660495

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: 95 SVs from 29 studies. See in: genome view

Submitted genomic72,609,864-72,609,864

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660495	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	72,609,864	72,609,864
nsv5660495	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	72,320,908	72,320,908

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17075863	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17075863	Submitted genomic		NC_000011.10:g.726 09864_72609865ins3 14	GRCh38 (hg38)		NC_000011.10	Chr11	72,609,864	72,609,864
nssv17075863	Remapped	Perfect	NC_000011.9:g.7232 0908_72320909ins31 4	GRCh37.p13	First Pass	NC_000011.9	Chr11	72,320,908	72,320,908

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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