A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698497



Internal ID15088463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12299150..12315975hg38UCSC Ensembl
Innerchr11:12320697..12337522hg19UCSC Ensembl
Innerchr11:12277273..12294098hg18UCSC Ensembl
Innerchr11:12277273..12294098hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3816826
hg1916826
hg1816826
hg1716826
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522844
Supporting Variants
Samples
Known GenesMICALCL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698497
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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