A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482746



Internal ID260194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91447634..91447729hg38UCSC Ensembl
chr7:91076949..91077044hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482746
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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