A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581473



Internal ID16368882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:37442344..37641071hg38UCSC Ensembl
Innerchr2:37669487..37868214hg19UCSC Ensembl
Innerchr2:37522991..37721718hg18UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38198728
hg19198728
hg18198728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151041
SamplesHGDP00880
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581473
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer