A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1146624



Internal ID15999810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133920718..133942161hg38UCSC Ensembl
Innerchr9:136785840..136807283hg19UCSC Ensembl
Innerchr9:135775661..135797104hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3821444
hg1921444
hg1821444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615741
Supporting Variants
Samples
Known GenesVAV2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1146624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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