A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584753



Internal ID18536348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:35840156..36398197hg38UCSC Ensembl
Innerchr20:34428078..35026600hg19UCSC Ensembl
Innerchr20:33891492..34460014hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38558042
hg19598523
hg18568523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066673
Supporting Variants
Samples
Known GenesAAR2, CNBD2, DLGAP4, EPB41L1, LINC00657, PHF20, SCAND1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584753
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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