A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701582



Internal ID15091548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49134487..49549035hg38UCSC Ensembl
Innerchr11:49156039..49570587hg19UCSC Ensembl
Innerchr11:49112615..49527163hg18UCSC Ensembl
Innerchr11:49112615..49527163hg17UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38414549
hg19414549
hg18414549
hg17414549
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525454
Supporting Variants
Samples
Known GenesFOLH1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701582
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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