A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059326



Internal ID18801857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:30710632..30870530hg38UCSC Ensembl
Innerchr21:32082950..32242849hg19UCSC Ensembl
Innerchr21:31004821..31164720hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38159899
hg19159900
hg18159900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4424n100
Supporting Variantsnssv3600117
Samples
Known GenesKRTAP21-1, KRTAP21-2, KRTAP21-3, KRTAP7-1, KRTAP8-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059326
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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