A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058157



Internal ID18800688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45729036..45749572hg38UCSC Ensembl
Innerchr20:44357675..44378211hg19UCSC Ensembl
Innerchr20:43791089..43811618hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3820537
hg1920537
hg1820530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584939, nssv3584936, nssv3584937, nssv3584940, nssv3584938
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)nsv1058157
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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