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dbVar

Database of genomic structural variation

nsv1154238

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:9

Description:Insertion of chrX:65588917-65588268
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: 170 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):168,546,049-168,546,057

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv1154238	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	168,546,049	168,546,057
nsv1154238	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	169,467,200	169,467,208

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv4004212	insertion	NA19701	Sequencing	Sequence alignment	5

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv4004212	Remapped	Perfect	NC_000004.12:g.(16 8546049_?)_(?_1685 46057)ins649	GRCh38.p12	First Pass	NC_000004.12	Chr4	168,546,049	168,546,057
nssv4004212	Submitted genomic		NC_000004.11:g.(16 9467200_?)_(?_1694 67208)ins649	GRCh37 (hg19)		NC_000004.11	Chr4	169,467,200	169,467,208

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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