A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015294



Internal ID19104511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17513285..17730195hg38UCSC Ensembl
Innerchr5:17513394..17730304hg19UCSC Ensembl
Innerchr5:17566394..17766033hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38216911
hg19216911
hg18199640
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638421
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)nsv1015294
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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