A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063852



Internal ID19153071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45897542..45938795hg38UCSC Ensembl
Innerchr21:47317456..47358709hg19UCSC Ensembl
Innerchr21:46141884..46183137hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3841254
hg1941254
hg1841254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4440n100
Supporting Variantsnssv3600302
Samples
Known GenesPCBP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063852
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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