A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614750



Internal ID16402159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81181252..81250303hg38UCSC Ensembl
Innerchr9:83796167..83865218hg19UCSC Ensembl
Innerchr9:82985987..83055038hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3869052
hg1969052
hg1869052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176457
Samples1780846029_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614750
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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