A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581019



Internal ID16368428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14177682..14242983hg38UCSC Ensembl
Innerchr2:14317807..14383107hg19UCSC Ensembl
Innerchr2:14235258..14300558hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3865302
hg1965301
hg1865301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903822
Samples
Known GenesLINC00276
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581019
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