A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522904



Internal ID15450197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5752388..5757156hg38UCSC Ensembl
Innerchr4:5754115..5758883hg19UCSC Ensembl
Innerchr4:5805016..5809784hg18UCSC Ensembl
Innerchr4:5872187..5876955hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg384769
hg194769
hg184769
hg174769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698562
Samples
Known GenesEVC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522904
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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