A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140771



Internal ID339964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133405236..133428946hg38UCSC Ensembl
chr6:133726374..133750084hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3823711
hg1923711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969504
Samples
Known GenesEYA4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140771
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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