A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176364



Internal ID15854371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89646949..89675959hg38UCSC Ensembl
Innerchr9:92261864..92290874hg19UCSC Ensembl
Innerchr9:91451684..91480694hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3829011
hg1929011
hg1829011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614850
Supporting Variants
Samples1780862093_A
Known GenesUNQ6494
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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