A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599352



Internal ID18897633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:4781931..4813599hg38UCSC Ensembl
Innerchr20:4762577..4794245hg19UCSC Ensembl
Innerchr20:4710577..4742245hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3831669
hg1931669
hg1831669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061866
Supporting Variants
Samples
Known GenesRASSF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599352
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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