A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676410



Internal ID15413062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9916998..9920885hg38UCSC Ensembl
Innerchr11:9938545..9942432hg19UCSC Ensembl
Innerchr11:9895121..9899008hg18UCSC Ensembl
Innerchr11:9895121..9899008hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383888
hg193888
hg183888
hg173888
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517092
Supporting Variants
Samples
Known GenesSBF2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676410
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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