A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527192



Internal ID15454485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:121843617..121848257hg38UCSC Ensembl
Innerchr9:124605896..124610536hg19UCSC Ensembl
Innerchr9:123645717..123650357hg18UCSC Ensembl
Innerchr9:121685450..121690090hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg384641
hg194641
hg184641
hg174641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703589
Samples
Known GenesMIR548AA1, MIR548D1, TTLL11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527192
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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