A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582169



Internal ID16369578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66709362..66732787hg38UCSC Ensembl
Innerchr2:66936494..66959919hg19UCSC Ensembl
Innerchr2:66789998..66813423hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3823426
hg1923426
hg1823426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911674
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582169
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer