A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032124



Internal ID19121346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:99583453..99666173hg38UCSC Ensembl
Innerchr5:98919157..99001877hg19UCSC Ensembl
Innerchr5:98947056..99029776hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3882721
hg1982721
hg1882721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5729n100
Supporting Variantsnssv3638066, nssv3638067
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)nsv1032124
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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