A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663772



Internal ID15053738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45878411..45881643hg38UCSC Ensembl
Innerchr11:45899962..45903194hg19UCSC Ensembl
Innerchr11:45856538..45859770hg18UCSC Ensembl
Innerchr11:45856538..45859770hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383233
hg193233
hg183233
hg173233
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516442
Supporting Variants
Samples
Known GenesCRY2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663772
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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