A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064215



Internal ID19153434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:22214829..22598130hg38UCSC Ensembl
Innerchr21:23587148..23970449hg19UCSC Ensembl
Innerchr21:22509019..22892320hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38383302
hg19383302
hg18383302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4404n100
Supporting Variantsnssv3732680
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)nsv1064215
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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