A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv849066



Internal ID16143022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:96106000..96112632hg38UCSC Ensembl
Innerchr15:96649229..96655861hg19UCSC Ensembl
Innerchr15:94450233..94456865hg18UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg386633
hg196633
hg186633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570574
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv849066
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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