A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581726



Internal ID16022449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45531486..45532516hg38UCSC Ensembl
Innerchr2:45758625..45759655hg19UCSC Ensembl
Innerchr2:45612129..45613159hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381031
hg191031
hg181031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6844n54
Supporting Variantsnssv908074
Samples
Known GenesSRBD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581726
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