A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470641



Internal ID248395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116836078..116836490hg38UCSC Ensembl
chr6:117157241..117157653hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470641
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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