A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615220



Internal ID16402629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113651471..113684601hg38UCSC Ensembl
Innerchr9:116413751..116446881hg19UCSC Ensembl
Innerchr9:115453572..115486702hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3833131
hg1933131
hg1833131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1141260
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615220
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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