A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176162



Internal ID15527557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136606710..136676165hg38UCSC Ensembl
Innerchr9:139501162..139570617hg19UCSC Ensembl
Innerchr9:138620983..138690438hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3869456
hg1969456
hg1869456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615977
Supporting Variants
SamplesHGDP00512
Known GenesAGPAT2, EGFL7, MIR126
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176162
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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