A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586079



Internal ID18884360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:53291517..53312291hg38UCSC Ensembl
Innerchr20:51908056..51928830hg19UCSC Ensembl
Innerchr20:51341463..51362237hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3820775
hg1920775
hg1820775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063840
Supporting Variants
Samples
Known GenesTSHZ2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586079
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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