A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642162



Internal ID18940443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:58014541..58036805hg38UCSC Ensembl
Innerchr5:57310368..57332632hg19UCSC Ensembl
Innerchr5:57346125..57368389hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3822265
hg1922265
hg1822265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019152
Supporting Variants
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)nssv3642162
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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