A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523940



Internal ID15104547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91784282..91811471hg38UCSC Ensembl
Innerchr9:94546564..94573753hg19UCSC Ensembl
Innerchr9:93586385..93613574hg18UCSC Ensembl
Innerchr9:91626119..91653308hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3827190
hg1927190
hg1827190
hg1727190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699786
Samples
Known GenesROR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523940
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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