A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710026



Internal ID15657296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12774110..12854043hg38UCSC Ensembl
Innerchr1:12834253..12913896hg19UCSC Ensembl
Innerchr1:12756840..12836483hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3879934
hg1979644
hg1879644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545449
Supporting Variants
Samples
Known GenesHNRNPCL1, LOC649330, PRAMEF1, PRAMEF11, PRAMEF12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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