A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141362



Internal ID340557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34686172..34686897hg38UCSC Ensembl
chr6:34653949..34654674hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980538
Samples
Known GenesC6orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141362
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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