A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141565



Internal ID340762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113534000..113539150hg38UCSC Ensembl
chr7:113174055..113179205hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg385151
hg195151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141565
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