A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613267



Internal ID16400676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7649442..7684552hg38UCSC Ensembl
Innerchr9:7649442..7684552hg19UCSC Ensembl
Innerchr9:7639442..7674552hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3835111
hg1935111
hg1835111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126856
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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