A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063479



Internal ID19152698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13197951..13718515hg38UCSC Ensembl
Innerchr21:14570272..15090836hg19UCSC Ensembl
Innerchr21:13492143..14012707hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38520565
hg19520565
hg18520565
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4381n100
Supporting Variantsnssv3585275
Samples
Known GenesLOC100288966, MIR3156-3, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063479
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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