A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1033362



Internal ID15886548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:60190941..60200348hg38UCSC Ensembl
Innerchr5:59486768..59496175hg19UCSC Ensembl
Innerchr5:59522525..59531932hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg389408
hg199408
hg189408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598262
Supporting Variants
Samples
Known GenesPDE4D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1033362
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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