A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018496



Internal ID19107713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:21005394..21325029hg38UCSC Ensembl
Innerchr5:21005503..21325138hg19UCSC Ensembl
Innerchr5:21041260..21360895hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38319636
hg19319636
hg18319636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5599n100
Supporting Variantsnssv3635924
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)nsv1018496
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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