A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv845271



Internal ID16139227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74417064..74418604hg38UCSC Ensembl
Innerchr15:74709405..74710945hg19UCSC Ensembl
Innerchr15:72496458..72497998hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381541
hg191541
hg181541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569977
Supporting Variants
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv845271
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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