A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614301



Internal ID16401710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:60994463..61002131hg38UCSC Ensembl
Innerchr9:39964959..39972620hg19UCSC Ensembl
Innerchr9:39954959..39962620hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg387669
hg197662
hg187662
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12694n54
Supporting Variantsnssv1134116, nssv1134117
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614301
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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