A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv987579



Internal ID15934849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1086705..1087309hg38UCSC Ensembl
Innerchr4:1080493..1081097hg19UCSC Ensembl
Innerchr4:1070493..1071097hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38605
hg19605
hg18605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593252
Supporting Variants
Samples
Known GenesRNF212
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv987579
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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