A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025807



Internal ID19115024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:59224224..59252405hg38UCSC Ensembl
Innerchr5:58520050..58548231hg19UCSC Ensembl
Innerchr5:58555807..58583988hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3828182
hg1928182
hg1828182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3640697, nssv3640695, nssv3640698, nssv3640696
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)nsv1025807
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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