A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712152



Internal ID15659422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:33254041..33354533hg38UCSC Ensembl
Innerchr1:33719642..33820134hg19UCSC Ensembl
Innerchr1:33492229..33592721hg18UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38100493
hg19100493
hg18100493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545963
Supporting Variants
Samples
Known GenesA3GALT2, MIR3605, PHC2, ZNF362
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712152
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