A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615064



Internal ID16055787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103811066..104367820hg38UCSC Ensembl
Innerchr9:106573347..107130101hg19UCSC Ensembl
Innerchr9:105613168..106169922hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38556755
hg19556755
hg18556755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1140802
Samples
Known GenesMIR6130, SMC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615064
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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