A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614598



Internal ID16402007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:70578455..70603740hg38UCSC Ensembl
Innerchr9:73193371..73218656hg19UCSC Ensembl
Innerchr9:72383191..72408476hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3825286
hg1925286
hg1825286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1137189
Samples
Known GenesTRPM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614598
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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