A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564199



Internal ID18515794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36586778..36613124hg38UCSC Ensembl
Innerchr18:34166741..34193087hg19UCSC Ensembl
Innerchr18:32420739..32447085hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3826347
hg1926347
hg1826347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067355
Supporting Variants
Samples
Known GenesFHOD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564199
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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