A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582806



Internal ID16370215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:121298108..121311598hg38UCSC Ensembl
Innerchr2:122055684..122069174hg19UCSC Ensembl
Innerchr2:121772154..121785644hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3813491
hg1913491
hg1813491
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916467
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582806
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