A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701042



Internal ID15091008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36456333..36457590hg38UCSC Ensembl
Innerchr18:34036296..34037553hg19UCSC Ensembl
Innerchr18:32290294..32291551hg18UCSC Ensembl
Innerchr18:32290294..32291551hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg381258
hg191258
hg181258
hg171258
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525007
Supporting Variants
Samples
Known GenesFHOD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701042
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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