A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015614



Internal ID19104831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:46152326..46334765hg38UCSC Ensembl
Innerchr5:46152428..46334867hg19UCSC Ensembl
Innerchr5:46188185..46370624hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38182440
hg19182440
hg18182440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5649n100
Supporting Variantsnssv3637974
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)nsv1015614
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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