A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056503



Internal ID18799034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35750468..35805624hg38UCSC Ensembl
Innerchr20:34338390..34393546hg19UCSC Ensembl
Innerchr20:33801804..33856960hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3855157
hg1955157
hg1855157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584751
Samples
Known GenesPHF20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056503
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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