A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701464



Internal ID15438116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:52929434..52929484hg38UCSC Ensembl
Innerchr4:53795601..53795651hg19UCSC Ensembl
Innerchr4:53490358..53490408hg18UCSC Ensembl
Innerchr4:53636529..53636579hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
hg1751
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525346
Supporting Variants
Samples
Known GenesSCFD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701464
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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