A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141305



Internal ID340500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112929332..112972433hg38UCSC Ensembl
chr6:113250534..113293635hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3843102
hg1943102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141305
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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