A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674234



Internal ID15410886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:51749599..51855992hg38UCSC Ensembl
Innerchr18:49275969..49382362hg19UCSC Ensembl
Innerchr18:47529967..47636360hg18UCSC Ensembl
Innerchr18:47529967..47636360hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38106394
hg19106394
hg18106394
hg17106394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520697
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674234
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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