A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491781



Internal ID269012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41805065..41810627hg38UCSC Ensembl
chr8:41662583..41668145hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg385563
hg195563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009736
Samples
Known GenesANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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