A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140816



Internal ID340009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119411381..119433000hg38UCSC Ensembl
chr4:120332536..120354155hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3821620
hg1921620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140816
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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