A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059241



Internal ID19148460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:51886511..51924566hg38UCSC Ensembl
Innerchr20:50503050..50541105hg19UCSC Ensembl
Innerchr20:49936457..49974512hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3838056
hg1938056
hg1838056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586073
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059241
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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