A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698190



Internal ID15088156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177090796..177174030hg38UCSC Ensembl
Innerchr5:176517797..176601031hg19UCSC Ensembl
Innerchr5:176450403..176533637hg18UCSC Ensembl
Innerchr5:176450403..176533637hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3883235
hg1983235
hg1883235
hg1783235
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521574
Supporting Variants
Samples
Known GenesFGFR4, NSD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698190
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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