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dbVar

Database of genomic structural variation

nsv1154236

Organism: Homo sapiens

Study:nstd105 (Onozawa et al. 2015)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:413

Description:Insertion of chrM:11763-11805
Publication(s):Onozawa et al. 2015

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: 134 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):68,238,594-68,239,006

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv1154236	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	68,238,594	68,239,006
nsv1154236	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	67,703,581	67,703,993

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv4004206	insertion	NA21767	Sequencing	Sequence alignment	5

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv4004206	Remapped	Perfect	NC_000007.14:g.(68 238594_?)_(?_68239 006)ins42	GRCh38.p12	First Pass	NC_000007.14	Chr7	68,238,594	68,239,006
nssv4004206	Submitted genomic		NC_000007.13:g.(67 703581_?)_(?_67703 993)ins42	GRCh37 (hg19)		NC_000007.13	Chr7	67,703,581	67,703,993

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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