A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615065



Internal ID16402474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103904926..104022781hg38UCSC Ensembl
Innerchr9:106667207..106785062hg19UCSC Ensembl
Innerchr9:105707028..105824883hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38117856
hg19117856
hg18117856
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140803
Samples
Known GenesMIR6130
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615065
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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