A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985292



Internal ID57594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85675390..85675686hg38UCSC Ensembl
chr6:86385108..86385404hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5472218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985292
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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