A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670554



Internal ID15407206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:55648827..55649601hg38UCSC Ensembl
Innerchr18:53316058..53316832hg19UCSC Ensembl
Innerchr18:51467056..51467830hg18UCSC Ensembl
Innerchr18:51467056..51467830hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38775
hg19775
hg18775
hg17775
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516739
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670554
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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