A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455172



Internal ID233254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35118848..35118924hg38UCSC Ensembl
chr6:35086625..35086701hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982084
Samples
Known GenesTCP11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455172
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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