A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063907



Internal ID18806438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45721722..45752208hg38UCSC Ensembl
Innerchr20:44350361..44380847hg19UCSC Ensembl
Innerchr20:43783775..43814254hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3830487
hg1930487
hg1830480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4321n100
Supporting Variantsnssv3584926
Samples
Known GenesSPINT4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063907
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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