A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584927



Internal ID18536522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45721722..45752976hg38UCSC Ensembl
Innerchr20:44350361..44381615hg19UCSC Ensembl
Innerchr20:43783775..43815022hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3831255
hg1931255
hg1831248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059109
Supporting Variants
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)nssv3584927
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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