A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569977



Internal ID16357386
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 StatusM
Merged Variantsdgv4624n54
Supporting Variantsnssv845271
Samples
Known GenesSEMA7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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