A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593558



Internal ID16380967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7107356..7135271hg38UCSC Ensembl
Innerchr4:7109083..7136998hg19UCSC Ensembl
Innerchr4:7159984..7187899hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3827916
hg1927916
hg1827916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv990872
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593558
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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