A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023502



Internal ID18766035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179659090..179678315hg38UCSC Ensembl
Innerchr5:179086091..179105316hg19UCSC Ensembl
Innerchr5:179018697..179037922hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3819226
hg1919226
hg1819226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649312
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023502
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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