A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055217



Internal ID19144436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16587417..16615825hg38UCSC Ensembl
Innerchr20:16568062..16596470hg19UCSC Ensembl
Innerchr20:16516062..16544470hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3828409
hg1928409
hg1828409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4280n100
Supporting Variantsnssv3584617
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)nsv1055217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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