A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562129



Internal ID335088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132165590..132167550hg38UCSC Ensembl
chr6:132486730..132488690hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg381961
hg191961
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970039
Samples
Known GenesLINC01013
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562129
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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