A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676509



Internal ID15413161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86057929..86068874hg38UCSC Ensembl
Innerchr4:86979082..86990027hg19UCSC Ensembl
Innerchr4:87198106..87209051hg18UCSC Ensembl
Innerchr4:87336261..87347206hg17UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3810946
hg1910946
hg1810946
hg1710946
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517318
Supporting Variants
Samples
Known GenesMAPK10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676509
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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