A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522707



Internal ID15450000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60561478..60649112hg38UCSC Ensembl
Innerchr18:58228711..58316345hg19UCSC Ensembl
Innerchr18:56379691..56467325hg18UCSC Ensembl
Innerchr18:56379691..56467325hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3887635
hg1987635
hg1887635
hg1787635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706119
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522707
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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