A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524118



Internal ID15451411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64298631..64351719hg38UCSC Ensembl
Innerchr6:65008524..65061612hg19UCSC Ensembl
Innerchr6:65066483..65119571hg18UCSC Ensembl
Innerchr6:65066483..65119571hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3853089
hg1953089
hg1853089
hg1753089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699996
Samples
Known GenesEYS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524118
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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