A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv587801



Internal ID16028524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44413029..44497025hg38UCSC Ensembl
Innerchr21:45832912..45916908hg19UCSC Ensembl
Innerchr21:44657340..44741336hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3883997
hg1983997
hg1883997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv948397
Samples
Known GenesLRRC3, LRRC3-AS1, TRPM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv587801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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