A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3640705



Internal ID18938986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:59377954..59490642hg38UCSC Ensembl
Innerchr5:58673780..58786468hg19UCSC Ensembl
Innerchr5:58709537..58822225hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38112689
hg19112689
hg18112689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028022
Supporting Variants
Samples
Known GenesPDE4D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3640705
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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