A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140551



Internal ID339744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27146588..27147536hg38UCSC Ensembl
chr6:27114367..27115315hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38949
hg19949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982436
Samples
Known GenesHIST1H2AH, HIST1H2BK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140551
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