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dbVar

Database of genomic structural variation

nsv5960551

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 118 SVs from 21 studies. See in: genome view

Submitted genomic98,436,304-98,436,304

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5960551	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	98,436,304	98,436,304
nsv5960551	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	101,198,586	101,198,586

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17430729	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17430729	Submitted genomic		NC_000009.12:g.984 36304_98436305ins5 2	GRCh38 (hg38)		NC_000009.12	Chr9	98,436,304	98,436,304
nssv17430729	Remapped	Perfect	NC_000009.11:g.101 198586_101198587in s52	GRCh37.p13	First Pass	NC_000009.11	Chr9	101,198,586	101,198,586

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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