A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524266



Internal ID15104873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96018324..96041992hg38UCSC Ensembl
Innerchr9:98780606..98804274hg19UCSC Ensembl
Innerchr9:97820427..97844095hg18UCSC Ensembl
Innerchr9:95860161..95883829hg17UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3823669
hg1923669
hg1823669
hg1723669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700163
Samples
Known GenesLINC00092
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524266
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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