A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615054



Internal ID16055777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103743412..104043599hg38UCSC Ensembl
Innerchr9:106505693..106805880hg19UCSC Ensembl
Innerchr9:105545514..105845701hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38300188
hg19300188
hg18300188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140627
Samples
Known GenesMIR6130
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615054
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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