A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058100



Internal ID18800631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52037708..52140042hg38UCSC Ensembl
Innerchr20:50654247..50756581hg19UCSC Ensembl
Innerchr20:50087654..50189988hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38102335
hg19102335
hg18102335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586075
Samples
Known GenesZFP64
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058100
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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