A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613429



Internal ID16400838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11453474..11645495hg38UCSC Ensembl
Innerchr9:11453474..11645495hg19UCSC Ensembl
Innerchr9:11443474..11635495hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38192022
hg19192022
hg18192022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12525n54
Supporting Variantsnssv1156681
SamplesHGDP00608
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613429
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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