A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657367



Internal ID15394019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22476030..22486192hg38UCSC Ensembl
Innerchr18:20055993..20066155hg19UCSC Ensembl
Innerchr18:18309991..18320153hg18UCSC Ensembl
Innerchr18:18309991..18320153hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810163
hg1910163
hg1810163
hg1710163
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515584
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657367
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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