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dbVar

Database of genomic structural variation

nsv6137148

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:translocation
Method Type:Sequencing
Submitted on:GRCh37

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

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

Remapped(Score: Perfect):199,757,872-199,757,872

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv6137148	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	199,757,872	199,757,872	+
nsv6137148	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	79,799,333	79,799,333	+
nsv6137148	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	199,727,000	199,727,000	+
nsv6137148	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	81,559,089	81,559,089	+

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17679581	interchromosomal translocation	SAMN20524662	Sequencing	Paired-end mapping	1,603

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv17679581	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	199,757,872	199,757,872	+
nssv17679581	Remapped	Perfect	GRCh38.p12	First Pass	NC_000010.11	Chr10	79,799,333	79,799,333	+
nssv17679581	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	199,727,000	199,727,000	+
nssv17679581	Submitted genomic		GRCh37 (hg19)		NC_000010.10	Chr10	81,559,089	81,559,089	+

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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