A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614877



Internal ID16402286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91640208..91640795hg38UCSC Ensembl
Innerchr9:94402490..94403077hg19UCSC Ensembl
Innerchr9:93442311..93442898hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38588
hg19588
hg18588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1139366, nssv1139365
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614877
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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