A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584726



Internal ID18536321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30290734..30416523hg38UCSC Ensembl
Innerchr20:29525410..29651199hg19UCSC Ensembl
Innerchr20:28139071..28264860hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38125790
hg19125790
hg18125790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067193
Supporting Variants
Samples
Known GenesFRG1B, MLLT10P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584726
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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