A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3734870



Internal ID19033151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7251313..7388261hg38UCSC Ensembl
Innerchr20:7231960..7368908hg19UCSC Ensembl
Innerchr20:7179960..7316908hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38136949
hg19136949
hg18136949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062870
Supporting Variants
Samples
Known GenesMIR8062
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3734870
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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