A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582524



Internal ID16369933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:99487290..99493891hg38UCSC Ensembl
Innerchr2:100103752..100110353hg19UCSC Ensembl
Innerchr2:99470184..99476785hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg386602
hg196602
hg186602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv914546
Samples
Known GenesREV1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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