A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176515



Internal ID15533650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133030314..133080285hg38UCSC Ensembl
Innerchr9:135905701..135955672hg19UCSC Ensembl
Innerchr9:134895522..134945493hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3849972
hg1949972
hg1849972
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615596
Supporting Variants
SamplesNINDS_197
Known GenesCEL, GTF3C5, MIR6877
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176515
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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