A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023545



Internal ID19112762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:36448793..36461229hg38UCSC Ensembl
Innerchr5:36448895..36461331hg19UCSC Ensembl
Innerchr5:36484652..36497088hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3812437
hg1912437
hg1812437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5631n100
Supporting Variantsnssv3745967, nssv3745966
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)nsv1023545
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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