A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700290



Internal ID15436942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10350831..10350890hg38UCSC Ensembl
Innerchr18:10350828..10350887hg19UCSC Ensembl
Innerchr18:10340828..10340887hg18UCSC Ensembl
Innerchr18:10340828..10340887hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3860
hg1960
hg1860
hg1760
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521207
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700290
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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