A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610697



Internal ID21802744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48427580..48427795hg38UCSC Ensembl
chr13:49001716..49001931hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027206
Supporting Variants
Samples
Known GenesLPAR6, RB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610697
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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