A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv851069



Internal ID16145025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101251057..101262360hg38UCSC Ensembl
Innerchr15:101791262..101802565hg19UCSC Ensembl
Innerchr15:99608785..99620088hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3811304
hg1911304
hg1811304
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv570844
Supporting Variants
Samples
Known GenesCHSY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv851069
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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