A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613206



Internal ID16400615
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 StatusM
Merged Variants
Supporting Variantsnssv1126535
Samples
Known GenesGLDC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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