A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063099



Internal ID18805630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:24646815..25225507hg38UCSC Ensembl
Innerchr21:26019129..26597821hg19UCSC Ensembl
Innerchr21:24941000..25519692hg18UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg38578693
hg19578693
hg18578693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732691
Samples
Known GenesLOC339622
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063099
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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