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dbVar

Database of genomic structural variation

nsv5966298

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

Submitted genomic13,310,637-13,310,637

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966298	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	13,310,637	13,310,637
nsv5966298	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	13,310,869	13,310,869

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17410612	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17410612	Submitted genomic		NC_000006.12:g.133 10637_13310638ins1 69	GRCh38 (hg38)		NC_000006.12	Chr6	13,310,637	13,310,637
nssv17410612	Remapped	Perfect	NC_000006.11:g.133 10869_13310870ins1 69	GRCh37.p13	First Pass	NC_000006.11	Chr6	13,310,869	13,310,869

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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