A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055577



Internal ID19144796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18876856..19018076hg38UCSC Ensembl
Innerchr21:20249174..20390395hg19UCSC Ensembl
Innerchr21:19171045..19312266hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38141221
hg19141222
hg18141222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732671
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)nsv1055577
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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