A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060508



Internal ID18803039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25937976..26324931hg38UCSC Ensembl
Innerchr20:25918612..26305567hg19UCSC Ensembl
Innerchr20:25866612..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38386956
hg19386956
hg18386956
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4292n100
Supporting Variantsnssv3584684, nssv3737185
Samples
Known GenesFAM182A, LOC100134868, LOC284801, MIR663A, NCOR1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060508
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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