A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569975



Internal ID16010698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74416730..74419428hg38UCSC Ensembl
Innerchr15:74709071..74711769hg19UCSC Ensembl
Innerchr15:72496124..72498822hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382699
hg192699
hg182699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4623n54
Supporting Variantsnssv845269
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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