A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176126



Internal ID15528811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113052193..113103993hg38UCSC Ensembl
Innerchr9:115814473..115866273hg19UCSC Ensembl
Innerchr9:114854294..114906094hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851801
hg1951801
hg1851801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615205
Supporting Variants
SamplesHGDP00692
Known GenesZFP37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176126
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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