A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526335



Internal ID15106942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110924073..110960441hg38UCSC Ensembl
Innerchr9:113686353..113722721hg19UCSC Ensembl
Innerchr9:112726174..112762542hg18UCSC Ensembl
Innerchr9:110765908..110802276hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3836369
hg1936369
hg1836369
hg1736369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702626
Samples
Known GenesLPAR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526335
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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