A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3640694



Internal ID18938975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:59190558..59242023hg38UCSC Ensembl
Innerchr5:58486384..58537849hg19UCSC Ensembl
Innerchr5:58522141..58573606hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3851466
hg1951466
hg1851466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023570
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)nssv3640694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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