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dbVar

Database of genomic structural variation

nsv1069193

Organism: Homo sapiens

Study:nstd99 (Thareja et al. 2015)
Variant Type:translocation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):Thareja 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: 144 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):119,659,499-119,659,499

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv1069193	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	119,659,499	119,659,499	not reported
nsv1069193	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	119,660,899	119,660,899	not reported
nsv1069193	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	120,417,075	120,417,075	not reported
nsv1069193	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	120,418,475	120,418,475	not reported

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3764122	intrachromosomal translocation	KWP1	Sequencing	Read depth and paired-end mapping	11,116

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv3764122	Remapped	Perfect	GRCh38.p12	First Pass	NC_000002.12	Chr2	119,659,499	119,659,499	not reported
nssv3764122	Remapped	Perfect	GRCh38.p12	First Pass	NC_000002.12	Chr2	119,660,899	119,660,899	not reported
nssv3764122	Submitted genomic		GRCh37 (hg19)		NC_000002.11	Chr2	120,417,075	120,417,075	not reported
nssv3764122	Submitted genomic		GRCh37 (hg19)		NC_000002.11	Chr2	120,418,475	120,418,475	not reported

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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