A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556903



Internal ID330023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:97309379..97332536hg38UCSC Ensembl
chr6:97757255..97780412hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3823158
hg1923158
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986961
Samples
Known GenesMIR548H3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556903
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer