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dbVar

Database of genomic structural variation

nsv5611901

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: 161 SVs from 31 studies. See in: genome view

Submitted genomic198,243,969-198,243,969

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5611901	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	198,243,969	198,243,969
nsv5611901	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	198,213,099	198,213,099

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17062345	insertion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17062345	Submitted genomic		NC_000001.11:g.198 243969_198243970in s321	GRCh38 (hg38)		NC_000001.11	Chr1	198,243,969	198,243,969
nssv17062345	Remapped	Perfect	NC_000001.10:g.198 213099_198213100in s321	GRCh37.p13	First Pass	NC_000001.10	Chr1	198,213,099	198,213,099

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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