A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3737187



Internal ID18688782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25978526..26324931hg38UCSC Ensembl
Innerchr20:25959162..26305567hg19UCSC Ensembl
Innerchr20:25907162..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38346406
hg19346406
hg18346406
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065198
Supporting Variants
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)nssv3737187
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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