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dbVar

Database of genomic structural variation

nsv4447436

Organism: Homo sapiens

Study:nstd175 (Genome in a Bottle)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Description:SVTYPE=INS;REPTYPE=SIMPLEINS
Publication(s):Genome in a Bottle

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: 115 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):30,623,727-30,623,727

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4447436	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	30,623,727	30,623,727
nsv4447436	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	31,019,714	31,019,714

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15759736	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15759736	Remapped	Perfect	NC_000022.11:g.306 23727_30623728ins3 86	GRCh38.p12	First Pass	NC_000022.11	Chr22	30,623,727	30,623,727
nssv15759736	Submitted genomic		NC_000022.10:g.310 19714_31019715ins3 86	GRCh37 (hg19)		NC_000022.10	Chr22	31,019,714	31,019,714

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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