A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525007



Internal ID15105614
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701042
Samples
Known GenesFHOD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525007
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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