A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527769



Internal ID15108376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36399448..36449208hg38UCSC Ensembl
Innerchr18:33979411..34029171hg19UCSC Ensembl
Innerchr18:32233409..32283169hg18UCSC Ensembl
Innerchr18:32233409..32283169hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3849761
hg1949761
hg1849761
hg1749761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704258
Samples
Known GenesFHOD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527769
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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