A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600219



Internal ID18551814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:43933555..43953423hg38UCSC Ensembl
Innerchr21:45353436..45373304hg19UCSC Ensembl
Innerchr21:44177864..44197732hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3819869
hg1919869
hg1819869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055772
Supporting Variants
Samples
Known GenesAGPAT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600219
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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