A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv848356



Internal ID15795626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90871778..90875361hg38UCSC Ensembl
Innerchr15:91415008..91418591hg19UCSC Ensembl
Innerchr15:89216012..89219595hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383584
hg193584
hg183584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570434
Supporting Variants
Samples
Known GenesFURIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv848356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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