A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064683



Internal ID18807214
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 StatusM
Merged Variantsdgv4390n100
Supporting Variantsnssv3586462
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)nsv1064683
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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