A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613395



Internal ID16400804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10649660..10686548hg38UCSC Ensembl
Innerchr9:10649660..10686548hg19UCSC Ensembl
Innerchr9:10639660..10676548hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3836889
hg1936889
hg1836889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12519n54
Supporting Variantsnssv1128515
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613395
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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