A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141770



Internal ID340967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11326681..11340014hg38UCSC Ensembl
chr8:11184190..11197523hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3813334
hg1913334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17008269
Samples
Known GenesMTMR9, SLC35G5, TDH
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141770
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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