A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569980



Internal ID16010703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74417225..74419290hg38UCSC Ensembl
Innerchr15:74709566..74711631hg19UCSC Ensembl
Innerchr15:72496619..72498684hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382066
hg192066
hg182066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4623n54
Supporting Variantsnssv845274
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569980
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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