A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521834



Internal ID15449127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:66256503..66259359hg38UCSC Ensembl
Innerchr2:66483635..66486491hg19UCSC Ensembl
Innerchr2:66337139..66339995hg18UCSC Ensembl
Innerchr2:66395286..66398142hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382857
hg192857
hg182857
hg172857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694607
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521834
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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