A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581719



Internal ID16022442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45531122..45532407hg38UCSC Ensembl
Innerchr2:45758261..45759546hg19UCSC Ensembl
Innerchr2:45611765..45613050hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381286
hg191286
hg181286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6843n54
Supporting Variantsnssv908055
Samples
Known GenesSRBD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581719
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