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dbVar

Database of genomic structural variation

nsv1154231

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:565

Description:Insertion of chrM:6220-6266
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: 226 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):173,936,142-173,936,706

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv1154231	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	173,936,142	173,936,706
nsv1154231	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	174,857,293	174,857,857

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv4004198	insertion	NA18502	Sequencing	Sequence alignment	5

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv4004198	Remapped	Perfect	NC_000004.12:g.(17 3936142_?)_(?_1739 36706)ins46	GRCh38.p12	First Pass	NC_000004.12	Chr4	173,936,142	173,936,706
nssv4004198	Submitted genomic		NC_000004.11:g.(17 4857293_?)_(?_1748 57857)ins46	GRCh37 (hg19)		NC_000004.11	Chr4	174,857,293	174,857,857

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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