A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613944



Internal ID16401353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27028949..27098942hg38UCSC Ensembl
Innerchr9:27028947..27098940hg19UCSC Ensembl
Innerchr9:27018947..27088940hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3869994
hg1969994
hg1869994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156748
SamplesHGDP00573
Known GenesIFT74
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613944
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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