A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065907



Internal ID19155126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:7775380..7813428hg38UCSC Ensembl
Innerchr20:7756027..7794075hg19UCSC Ensembl
Innerchr20:7704027..7742075hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3838049
hg1938049
hg1838049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599363
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)nsv1065907
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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