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dbVar

Database of genomic structural variation

nsv5970593

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: 424 SVs from 27 studies. See in: genome view

Submitted genomic70,342,241-70,342,241

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5970593	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	70,342,241	70,342,241
nsv5970593	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	68,009,477	68,009,477

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17399688	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17399688	Submitted genomic		NC_000018.10:g.703 42241_70342242ins7 6	GRCh38 (hg38)		NC_000018.10	Chr18	70,342,241	70,342,241
nssv17399688	Remapped	Perfect	NC_000018.9:g.6800 9477_68009478ins76	GRCh37.p13	First Pass	NC_000018.9	Chr18	68,009,477	68,009,477

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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