A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458903



Internal ID236923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167155513..167512188hg38UCSC Ensembl
chr6:167569001..167924380hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38356676
hg19355380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991257
Samples
Known GenesGPR31, TCP10, TCP10L2, TTLL2, UNC93A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458903
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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