A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525699



Internal ID15452992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48817295..48820834hg38UCSC Ensembl
Innerchr18:46343666..46347205hg19UCSC Ensembl
Innerchr18:44597664..44601203hg18UCSC Ensembl
Innerchr18:44597664..44601203hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg383540
hg193540
hg183540
hg173540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701859
Samples
Known GenesCTIF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525699
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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