A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033240



Internal ID19122462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:30297170..30435088hg38UCSC Ensembl
Innerchr5:30297277..30435195hg19UCSC Ensembl
Innerchr5:30333034..30470952hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38137919
hg19137919
hg18137919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5617n100
Supporting Variantsnssv3636024
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)nsv1033240
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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