A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060746



Internal ID19149965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:21905446..22027595hg38UCSC Ensembl
Innerchr21:23277766..23399914hg19UCSC Ensembl
Innerchr21:22199637..22321785hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38122150
hg19122149
hg18122149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732678
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)nsv1060746
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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