A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700168



Internal ID15090134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117180449..117214554hg38UCSC Ensembl
Innerchr11:117051165..117085270hg19UCSC Ensembl
Innerchr11:116556375..116590480hg18UCSC Ensembl
Innerchr11:116556375..116590480hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3834106
hg1934106
hg1834106
hg1734106
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524270
Supporting Variants
Samples
Known GenesLOC100652768, PCSK7, SIDT2, TAGLN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700168
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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