A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700483



Internal ID15437135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11670846..11683432hg38UCSC Ensembl
Innerchr18:11670845..11683431hg19UCSC Ensembl
Innerchr18:11660845..11673431hg18UCSC Ensembl
Innerchr18:11660845..11673431hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3812587
hg1912587
hg1812587
hg1712587
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524533
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700483
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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