A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695412



Internal ID15432064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:65545921..65608005hg38UCSC Ensembl
Innerchr18:63213157..63275241hg19UCSC Ensembl
Innerchr18:61364137..61426221hg18UCSC Ensembl
Innerchr18:61364137..61426221hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3862085
hg1962085
hg1862085
hg1762085
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518000
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695412
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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