A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1126535



Internal ID15979721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6525753..6686738hg38UCSC Ensembl
Innerchr9:6525753..6686738hg19UCSC Ensembl
Innerchr9:6515753..6676738hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38160986
hg19160986
hg18160986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv613206
Supporting Variants
Samples
Known GenesGLDC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1126535
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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