A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582554



Internal ID16023277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:102061304..102074850hg38UCSC Ensembl
Innerchr2:102677765..102691310hg19UCSC Ensembl
Innerchr2:102044197..102057742hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3813547
hg1913546
hg1813546
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6981n54
Supporting Variantsnssv914700
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582554
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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