A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518093



Internal ID15445386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76014023..76027279hg38UCSC Ensembl
Innerchr6:76723740..76736996hg19UCSC Ensembl
Innerchr6:76780460..76793716hg18UCSC Ensembl
Innerchr6:76780460..76793716hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3813257
hg1913257
hg1813257
hg1713257
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695505
Samples
Known GenesIMPG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518093
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