A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015679



Internal ID19104897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:5125846..5154345hg38UCSC Ensembl
Innerchr5:5125959..5154458hg19UCSC Ensembl
Innerchr5:5178959..5207458hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3828500
hg1928500
hg1828500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638530
Samples
Known GenesADAMTS16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015679
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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