A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055772



Internal ID18798303
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 StatusM
Merged Variants
Supporting Variantsnssv3600219
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)nsv1055772
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer