A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525442



Internal ID15452735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122090007..122123317hg38UCSC Ensembl
Innerchr9:124852286..124885596hg19UCSC Ensembl
Innerchr9:123892107..123925417hg18UCSC Ensembl
Innerchr9:121931840..121965150hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3833311
hg1933311
hg1833311
hg1733311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701570
Samples
Known GenesMIR4478, TTLL11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525442
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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