A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581479



Internal ID16368888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38151968..38177244hg38UCSC Ensembl
Innerchr2:38379110..38404386hg19UCSC Ensembl
Innerchr2:38232614..38257890hg18UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3825277
hg1925277
hg1825277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6788n54
Supporting Variantsnssv906868
Samples
Known GenesCYP1B1-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581479
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