A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176363



Internal ID15879217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88428330..88494583hg38UCSC Ensembl
Innerchr9:91043245..91109498hg19UCSC Ensembl
Innerchr9:90233065..90299318hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3866254
hg1966254
hg1866254
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614807
Supporting Variants
SamplesHGDP01329
Known GenesSPIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176363
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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