A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587810



Internal ID16028533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44572258..44627716hg38UCSC Ensembl
Innerchr21:45992131..46047633hg19UCSC Ensembl
Innerchr21:44816559..44872061hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3855459
hg1955503
hg1855503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948406
Samples
Known GenesKRTAP10-4, KRTAP10-5, KRTAP10-6, KRTAP10-7, KRTAP10-8, KRTAP10-9, TSPEAR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587810
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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