A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057093



Internal ID19146312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22061780..22173462hg38UCSC Ensembl
Innerchr20:22042418..22154100hg19UCSC Ensembl
Innerchr20:21990418..22102100hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38111683
hg19111683
hg18111683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4285n100
Supporting Variantsnssv3584654, nssv3584653
Samples
Known GenesLOC100270679
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057093
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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