A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614955



Internal ID16055678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:100419314..100498945hg38UCSC Ensembl
Innerchr9:103181596..103261227hg19UCSC Ensembl
Innerchr9:102221417..102301048hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3879632
hg1979632
hg1879632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140215
Samples
Known GenesMSANTD3, MSANTD3-TMEFF1, TMEFF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614955
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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