Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6137500

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: 122 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):7,901,145-7,901,145

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv6137500	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	7,901,145	7,901,145	+
nsv6137500	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	37,573,186	37,573,186	+
nsv6137500	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	7,940,776	7,940,776	+
nsv6137500	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	38,042,391	38,042,391	+

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17681393	interchromosomal translocation	SAMN20524660	Sequencing	Paired-end mapping	208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv17681393	Remapped	Perfect	GRCh38.p12	First Pass	NC_000007.14	Chr7	7,901,145	7,901,145	+
nssv17681393	Remapped	Perfect	GRCh38.p12	First Pass	NC_000014.9	Chr14	37,573,186	37,573,186	+
nssv17681393	Submitted genomic		GRCh37 (hg19)		NC_000007.13	Chr7	7,940,776	7,940,776	+
nssv17681393	Submitted genomic		GRCh37 (hg19)		NC_000014.8	Chr14	38,042,391	38,042,391	+

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

You are here: NCBI