A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615428



Internal ID16402837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129384126..129419493hg38UCSC Ensembl
Innerchr9:132146405..132181772hg19UCSC Ensembl
Innerchr9:131186226..131221593hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3835368
hg1935368
hg1835368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12891n54
Supporting Variantsnssv1144780
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615428
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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