A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468731



Internal ID246525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26250264..26251875hg38UCSC Ensembl
chr6:26250492..26252103hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381612
hg191612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982370
Samples
Known GenesHIST1H2BH, HIST1H3F
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468731
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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