A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558566



Internal ID331625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15708864..15862967hg38UCSC Ensembl
chr7:15748489..15902592hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38154104
hg19154104
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558566
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