A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455021



Internal ID233112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70338929..70355354hg38UCSC Ensembl
chr6:71048632..71065057hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3816426
hg1916426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455021
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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