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

dbVar

Database of genomic structural variation

nsv4715847

Organism: Homo sapiens

Study:nstd195 (Mwapagha et al. 2021)
Variant Type:translocation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):Mwapagha et al. 2021

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: 128 SVs from 32 studies. See in: genome view

Remapped(Score: Perfect):30,935,527-30,935,527

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv4715847	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	30,935,527	30,935,527	-
nsv4715847	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	67,342,438	67,342,438	-
nsv4715847	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	30,957,074	30,957,074	-
nsv4715847	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	67,916,570	67,916,570	-

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Copy number	Other Calls in this Sample and Study
nssv16234773	interchromosomal translocation	M456	Sequencing	Paired-end mapping	1	4,735

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv16234773	Remapped	Perfect	GRCh38.p12	First Pass	NC_000011.10	Chr11	30,935,527	30,935,527	-
nssv16234773	Remapped	Perfect	GRCh38.p12	First Pass	NC_000013.11	Chr13	67,342,438	67,342,438	-
nssv16234773	Submitted genomic		GRCh37 (hg19)		NC_000011.9	Chr11	30,957,074	30,957,074	-
nssv16234773	Submitted genomic		GRCh37 (hg19)		NC_000013.10	Chr13	67,916,570	67,916,570	-

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI