A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593532



Internal ID16380941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6782340..6809193hg38UCSC Ensembl
Innerchr4:6784067..6810920hg19UCSC Ensembl
Innerchr4:6834968..6861821hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3826854
hg1926854
hg1826854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv990237
Samples
Known GenesKIAA0232
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593532
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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