A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019152



Internal ID19108370
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 StatusM
Merged Variantsdgv5673n100
Supporting Variantsnssv3642161, nssv3642162
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)nsv1019152
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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