A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703682



Internal ID15440334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59072943..59077434hg38UCSC Ensembl
Innerchr18:56740175..56744666hg19UCSC Ensembl
Innerchr18:54891155..54895646hg18UCSC Ensembl
Innerchr18:54891155..54895646hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg384492
hg194492
hg184492
hg174492
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527272
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703682
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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