A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064436



Internal ID18806967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38474648..38503652hg38UCSC Ensembl
Innerchr21:39846571..39875576hg19UCSC Ensembl
Innerchr21:38768441..38797446hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3829005
hg1929006
hg1829006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600194
Samples
Known GenesERG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064436
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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