A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064806



Internal ID19154025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:12992198..13013692hg38UCSC Ensembl
Innerchr21:14364519..14386013hg19UCSC Ensembl
Innerchr21:13286390..13307884hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3821495
hg1921495
hg1821495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3585214, nssv3585215
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)nsv1064806
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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