A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521938



Internal ID15102545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56748122..56888242hg38UCSC Ensembl
Innerchr18:54415353..54555473hg19UCSC Ensembl
Innerchr18:52566351..52706471hg18UCSC Ensembl
Innerchr18:52566351..52706471hg17UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38140121
hg19140121
hg18140121
hg17140121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694707
Samples
Known GenesWDR7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521938
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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