A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673866



Internal ID15410518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76143191..76149135hg38UCSC Ensembl
Innerchr11:75854235..75860179hg19UCSC Ensembl
Innerchr11:75531883..75537827hg18UCSC Ensembl
Innerchr11:75531883..75537827hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg385945
hg195945
hg185945
hg175945
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515484
Supporting Variants
Samples
Known GenesUVRAG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673866
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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