A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587342



Internal ID16374751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:27171137..28110169hg38UCSC Ensembl
Innerchr21:28543456..29482488hg19UCSC Ensembl
Innerchr21:27465327..28404359hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38939033
hg19939033
hg18939033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151604
Samples1780862076_A
Known GenesLINC00113, LINC00314, MIR5009
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587342
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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