A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557047



Internal ID330163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6350680..6355845hg38UCSC Ensembl
chr5:6350793..6355958hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385166
hg195166
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961909
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557047
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