A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589652



Internal ID16030375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10427039..10466687hg38UCSC Ensembl
Innerchr3:10468723..10508371hg19UCSC Ensembl
Innerchr3:10443723..10483371hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3839649
hg1939649
hg1839649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958899
Samples
Known GenesATP2B2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589652
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