A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454813



Internal ID232907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163144074..163146304hg38UCSC Ensembl
chr6:163565106..163567336hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382231
hg192231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990914
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454813
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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