A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524049



Internal ID6021519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73612833..73680301hg19UCSC Ensembl
Innerchr15:71399886..71467354hg18UCSC Ensembl
Innerchr15:71399886..71467354hg17UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv699913
Samples
Known GenesHCN4
Method
AnalysisCNV regions located outside of or spanning over several merged-level regions determined by the submitter
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv524049
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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