A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1139364



Internal ID15992550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91640140..91641031hg38UCSC Ensembl
Innerchr9:94402422..94403313hg19UCSC Ensembl
Innerchr9:93442243..93443134hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38892
hg19892
hg18892
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614876
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1139364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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