A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140859



Internal ID340053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105171382..105172911hg38UCSC Ensembl
chr6:105619257..105620786hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987846
Samples
Known GenesPOPDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140859
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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