A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589960



Internal ID18541555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:567543..606311hg38UCSC Ensembl
Innerchr20:548187..586955hg19UCSC Ensembl
Innerchr20:496187..534955hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838769
hg1938769
hg1838769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058681
Supporting Variants
Samples
Known GenesTCF15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589960
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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