A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984989



Internal ID57383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87429244..87433587hg38UCSC Ensembl
chr6:88138962..88143305hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384344
hg194344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457310
Supporting Variants
Samples
Known GenesC6orf165
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984989
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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