A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066430



Internal ID19155649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13221902..13761359hg38UCSC Ensembl
Innerchr21:14594223..15133680hg19UCSC Ensembl
Innerchr21:13516094..14055551hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38539458
hg19539458
hg18539458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4381n100
Supporting Variantsnssv3585292, nssv3585291, nssv3585293
Samples
Known GenesLOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066430
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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