A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3731501



Internal ID19029782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60989035..61015539hg38UCSC Ensembl
Innerchr20:59564091..59590595hg19UCSC Ensembl
Innerchr20:58997486..59023990hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3826505
hg1926505
hg1826505
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062229
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3731501
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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