A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525589



Internal ID15106196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10078838..10098190hg38UCSC Ensembl
Innerchr4:10080462..10099814hg19UCSC Ensembl
Innerchr4:9689560..9708912hg18UCSC Ensembl
Innerchr4:9756731..9776083hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3819353
hg1919353
hg1819353
hg1719353
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701728
Samples
Known GenesWDR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525589
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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