A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468208



Internal ID246010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56391293..56401636hg38UCSC Ensembl
chr6:56256091..56266434hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3810344
hg1910344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982910
Samples
Known GenesRNU6-71P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468208
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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