A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581611



Internal ID16369020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:42047426..42048237hg38UCSC Ensembl
Innerchr2:42274566..42275377hg19UCSC Ensembl
Innerchr2:42128070..42128881hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38812
hg19812
hg18812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6818n54
Supporting Variantsnssv907425
Samples
Known GenesPKDCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581611
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