A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615032



Internal ID16402441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102565313..102681278hg38UCSC Ensembl
Innerchr9:105327595..105443560hg19UCSC Ensembl
Innerchr9:104367416..104483381hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38115966
hg19115966
hg18115966
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140611
Samples
Known GenesLINC00587
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615032
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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