A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3638530



Internal ID18936811
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 StatusS
Merged Variantsnsv1015679
Supporting Variants
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)nssv3638530
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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