A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614858



Internal ID16402267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91633240..91640846hg38UCSC Ensembl
Innerchr9:94395522..94403128hg19UCSC Ensembl
Innerchr9:93435343..93442949hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg387607
hg197607
hg187607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12792n54
Supporting Variantsnssv1139323
Samples
Known GenesMIR3910-1, MIR3910-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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