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dbVar

Database of genomic structural variation

nsv5969341

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: 114 SVs from 25 studies. See in: genome view

Submitted genomic30,623,921-30,623,921

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5969341	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	30,623,921	30,623,921
nsv5969341	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	31,019,908	31,019,908

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17397715	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17397715	Submitted genomic		NC_000022.11:g.306 23921_30623922ins2 04	GRCh38 (hg38)		NC_000022.11	Chr22	30,623,921	30,623,921
nssv17397715	Remapped	Perfect	NC_000022.10:g.310 19908_31019909ins2 04	GRCh37.p13	First Pass	NC_000022.10	Chr22	31,019,908	31,019,908

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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