A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527206



Internal ID15107813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92521930..92522700hg38UCSC Ensembl
Innerchr9:95284212..95284982hg19UCSC Ensembl
Innerchr9:94324033..94324803hg18UCSC Ensembl
Innerchr9:92363767..92364537hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38771
hg19771
hg18771
hg17771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703606
Samples
Known GenesCENPP, ECM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527206
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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