A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523287



Internal ID15103894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101429110..101440521hg38UCSC Ensembl
Innerchr9:104191392..104202803hg19UCSC Ensembl
Innerchr9:103231213..103242624hg18UCSC Ensembl
Innerchr9:101270947..101282358hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3811412
hg1911412
hg1811412
hg1711412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699026
Samples
Known GenesALDOB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523287
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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