A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176447



Internal ID15880932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36856271..36885586hg38UCSC Ensembl
Innerchr9:36856268..36885583hg19UCSC Ensembl
Innerchr9:36846268..36875583hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3829316
hg1929316
hg1829316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614212
Supporting Variants
SamplesNINDS_49
Known GenesMIR4540, PAX5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176447
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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