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dbVar

Database of genomic structural variation

nsv5672458

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: 86 SVs from 22 studies. See in: genome view

Submitted genomic58,615,880-58,615,880

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5672458	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	58,615,880	58,615,880
nsv5672458	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	57,190,936	57,190,936

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17117154	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17117154	Submitted genomic		NC_000020.11:g.586 15880_58615881ins7 6	GRCh38 (hg38)		NC_000020.11	Chr20	58,615,880	58,615,880
nssv17117154	Remapped	Perfect	NC_000020.10:g.571 90936_57190937ins7 6	GRCh37.p13	First Pass	NC_000020.10	Chr20	57,190,936	57,190,936

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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