A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461408



Internal ID239362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100851709..100851805hg38UCSC Ensembl
chr6:101299585..101299681hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987044
Samples
Known GenesASCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461408
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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