A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701193



Internal ID15437845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59012267..59027547hg38UCSC Ensembl
Innerchr18:56679499..56694779hg19UCSC Ensembl
Innerchr18:54830479..54845759hg18UCSC Ensembl
Innerchr18:54830479..54845759hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3815281
hg1915281
hg1815281
hg1715281
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525125
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701193
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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