A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669740



Internal ID15406392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17794865..17799635hg38UCSC Ensembl
Innerchr11:17816412..17821182hg19UCSC Ensembl
Innerchr11:17772988..17777758hg18UCSC Ensembl
Innerchr11:17772988..17777758hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384771
hg194771
hg184771
hg174771
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515890
Supporting Variants
Samples
Known GenesSERGEF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669740
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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