A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176456



Internal ID15880322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:80870671..80909312hg38UCSC Ensembl
Innerchr9:83485586..83524227hg19UCSC Ensembl
Innerchr9:82675406..82714047hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3838642
hg1938642
hg1838642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614749
Supporting Variants
SamplesNINDS_195
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176456
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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