A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460112



Internal ID238106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106738631..106738685hg38UCSC Ensembl
chr6:107186506..107186560hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986316
Samples
Known GenesLOC100422737
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460112
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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