A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024157



Internal ID19113374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:73252650..73408288hg38UCSC Ensembl
Innerchr5:72548477..72704115hg19UCSC Ensembl
Innerchr5:72584233..72739871hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38155639
hg19155639
hg18155639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641071
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)nsv1024157
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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