A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062229



Internal ID19151448
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 StatusM
Merged Variantsdgv4340n100
Supporting Variantsnssv3731501
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)nsv1062229
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer