A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515808



Internal ID15096415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53990691..54000869hg38UCSC Ensembl
Innerchr6:53855489..53865667hg19UCSC Ensembl
Innerchr6:53963448..53973626hg18UCSC Ensembl
Innerchr6:53963448..53973626hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3810179
hg1910179
hg1810179
hg1710179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656848, nssv688133, nssv664836
Samples
Known GenesMLIP-IT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515808
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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