A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615204



Internal ID16402613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113013459..113053118hg38UCSC Ensembl
Innerchr9:115775739..115815398hg19UCSC Ensembl
Innerchr9:114815560..114855219hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3839660
hg1939660
hg1839660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141246
Samples
Known GenesZFP37
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615204
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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