A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525736



Internal ID15106343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111384406..111386604hg38UCSC Ensembl
Innerchr9:114146686..114148884hg19UCSC Ensembl
Innerchr9:113186507..113188705hg18UCSC Ensembl
Innerchr9:111226241..111228439hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
hg172199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701901
Samples
Known GenesKIAA0368
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525736
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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