A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469078



Internal ID246871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34130993..34131080hg38UCSC Ensembl
chr6:34098770..34098857hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982034
Samples
Known GenesGRM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469078
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