A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582267



Internal ID16369676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77792218..77821639hg38UCSC Ensembl
Innerchr2:78019344..78048765hg19UCSC Ensembl
Innerchr2:77872852..77902273hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3829422
hg1929422
hg1829422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150239
SamplesHGDP01318
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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