A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468386



Internal ID246184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3955608..3957580hg38UCSC Ensembl
chr6:3955842..3957814hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381973
hg191973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468386
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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