A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615195



Internal ID16402604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112061018..112095922hg38UCSC Ensembl
Innerchr9:114823298..114858202hg19UCSC Ensembl
Innerchr9:113863119..113898023hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3834905
hg1934905
hg1834905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141242
Samples
Known GenesMIR3134, SUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615195
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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