A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063840



Internal ID19153059
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 StatusM
Merged Variants
Supporting Variantsnssv3586080, nssv3586079, nssv3586078
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)nsv1063840
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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