A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv838770



Internal ID16132726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:25087053..25088823hg38UCSC Ensembl
Innerchr15:25332200..25333970hg19UCSC Ensembl
Innerchr15:22883293..22885063hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381771
hg191771
hg181771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568536
Supporting Variants
Samples
Known GenesSNORD116-20, SNORD116-21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv838770
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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