A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586462



Internal ID18538057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15582251..15773439hg38UCSC Ensembl
Innerchr21:16954570..17145758hg19UCSC Ensembl
Innerchr21:15876441..16067629hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38191189
hg19191189
hg18191189
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064683
Supporting Variants
Samples
Known GenesUSP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586462
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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