A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614657



Internal ID16402066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73961328..74111519hg38UCSC Ensembl
Innerchr9:76576244..76726435hg19UCSC Ensembl
Innerchr9:75766064..75916255hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38150192
hg19150192
hg18150192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137322
Samples
Known GenesMIR6130
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614657
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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