A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523562



Internal ID15450855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91029128..91037735hg38UCSC Ensembl
Innerchr9:93791410..93800017hg19UCSC Ensembl
Innerchr9:92831231..92839838hg18UCSC Ensembl
Innerchr9:90870965..90879572hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg388608
hg198608
hg188608
hg178608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699343
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523562
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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