A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176102



Internal ID15874840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103476643..103541971hg38UCSC Ensembl
Innerchr9:106238925..106304253hg19UCSC Ensembl
Innerchr9:105278746..105344074hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3865329
hg1965329
hg1865329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615048
Supporting Variants
SamplesHGDP00599
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176102
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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