A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702007



Internal ID15438659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62879828..62926259hg38UCSC Ensembl
Innerchr18:60547061..60593492hg19UCSC Ensembl
Innerchr18:58698041..58744472hg18UCSC Ensembl
Innerchr18:58698041..58744472hg17UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3846432
hg1946432
hg1846432
hg1746432
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525821
Supporting Variants
Samples
Known GenesPHLPP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702007
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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