A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688539



Internal ID15425191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121844915..121845424hg38UCSC Ensembl
Innerchr9:124607194..124607703hg19UCSC Ensembl
Innerchr9:123647015..123647524hg18UCSC Ensembl
Innerchr9:121686748..121687257hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38510
hg19510
hg18510
hg17510
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521251
Supporting Variants
Samples
Known GenesMIR548AA1, MIR548D1, TTLL11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688539
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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