A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057185



Internal ID19146404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13221902..13850539hg38UCSC Ensembl
Innerchr21:14594223..15222860hg19UCSC Ensembl
Innerchr21:13516094..14144731hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38628638
hg19628638
hg18628638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4381n100
Supporting Variantsnssv3732588, nssv3585302
Samples
Known GenesC21orf15, LOC100288966, 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)nsv1057185
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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