A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1059615



Internal ID15566115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52752446..52809153hg38UCSC Ensembl
Innerchr6:52617244..52673951hg19UCSC Ensembl
Innerchr6:52725203..52781910hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3856708
hg1956708
hg1856708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv603108
Supporting Variants
Samples
Known GenesGSTA1, GSTA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1059615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer