A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702779



Internal ID15439431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78773765..78775692hg38UCSC Ensembl
Innerchr18:76533765..76535692hg19UCSC Ensembl
Innerchr18:74634753..74636680hg18UCSC Ensembl
Innerchr18:74634753..74636680hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381928
hg191928
hg181928
hg171928
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526473
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702779
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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