A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614850



Internal ID16402259
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 StatusM
Merged Variants
Supporting Variantsnssv1139316, nssv1176364
Samples1780862093_A
Known GenesUNQ6494
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614850
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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