A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156451



Internal ID15876238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:20508505..20548239hg38UCSC Ensembl
Innerchr9:20508503..20548238hg19UCSC Ensembl
Innerchr9:20498503..20538238hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3839735
hg1939736
hg1839736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613746
Supporting Variants
SamplesHGDP00806
Known GenesMLLT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156451
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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