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dbVar

Database of genomic structural variation

nsv5634101

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: 97 SVs from 24 studies. See in: genome view

Submitted genomic39,334,534-39,334,534

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5634101	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	39,334,534	39,334,534
nsv5634101	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	39,334,636	39,334,636

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17123297	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
nssv17123297	Submitted genomic		NC_000005.10:g.393 34534_39334535ins8 0	GRCh38 (hg38)		NC_000005.10	Chr5	39,334,534	39,334,534
nssv17123297	Remapped	Perfect	NC_000005.9:g.3933 4636_39334637ins80	GRCh37.p13	First Pass	NC_000005.9	Chr5	39,334,636	39,334,636

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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