A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059500



Internal ID18802031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:15585433..15773439hg38UCSC Ensembl
Innerchr21:16957752..17145758hg19UCSC Ensembl
Innerchr21:15879623..16067629hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38188007
hg19188007
hg18188007
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4390n100
Supporting Variantsnssv3586463
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)nsv1059500
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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