A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524687



Internal ID15105294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10078838..10157479hg38UCSC Ensembl
Innerchr4:10080462..10159103hg19UCSC Ensembl
Innerchr4:9689560..9768201hg18UCSC Ensembl
Innerchr4:9756731..9835372hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3878642
hg1978642
hg1878642
hg1778642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700659
Samples
Known GenesWDR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524687
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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