A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032430



Internal ID19121652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120710957..120886433hg38UCSC Ensembl
Innerchr5:120046652..120222128hg19UCSC Ensembl
Innerchr5:120074551..120250027hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38175477
hg19175477
hg18175477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5798n100
Supporting Variantsnssv3647988
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)nsv1032430
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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