A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702915



Internal ID15092881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36653268..36653679hg38UCSC Ensembl
Innerchr18:34233231..34233642hg19UCSC Ensembl
Innerchr18:32487229..32487640hg18UCSC Ensembl
Innerchr18:32487229..32487640hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38412
hg19412
hg18412
hg17412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526596
Supporting Variants
Samples
Known GenesFHOD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702915
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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