A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699708



Internal ID15436360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76256651..76256797hg38UCSC Ensembl
Innerchr11:75967695..75967841hg19UCSC Ensembl
Innerchr11:75645343..75645489hg18UCSC Ensembl
Innerchr11:75645343..75645489hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38147
hg19147
hg18147
hg17147
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523869
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699708
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