A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701728



Internal ID15091694
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525589
Supporting Variants
Samples
Known GenesWDR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701728
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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