A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569987



Internal ID16010710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74427735..74429720hg38UCSC Ensembl
Innerchr15:74720076..74722061hg19UCSC Ensembl
Innerchr15:72507129..72509114hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381986
hg191986
hg181986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845281
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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