A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697574



Internal ID15434226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:59224909..59262562hg38UCSC Ensembl
Innerchr5:58520735..58558388hg19UCSC Ensembl
Innerchr5:58556492..58594145hg18UCSC Ensembl
Innerchr5:58556492..58594145hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3837654
hg1937654
hg1837654
hg1737654
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520721
Supporting Variants
Samples
Known GenesPDE4D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697574
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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