A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267780



Internal ID20476998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90976291..90976364hg38UCSC Ensembl
chr15:91519521..91519594hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746266
Supporting Variants
Samples
Known GenesPRC1, PRC1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267780
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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