A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv845272



Internal ID16139228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74417064..74418781hg38UCSC Ensembl
Innerchr15:74709405..74711122hg19UCSC Ensembl
Innerchr15:72496458..72498175hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381718
hg191718
hg181718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569978
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)nssv845272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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