A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059145



Internal ID19148364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5752029..5843483hg38UCSC Ensembl
Innerchr20:5732675..5824129hg19UCSC Ensembl
Innerchr20:5680675..5772129hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3891455
hg1991455
hg1891455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734869
Samples
Known GenesC20orf196
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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