A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144074



Internal ID343277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90076896..90093300hg38UCSC Ensembl
chr11:89810064..89826468hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3816405
hg1916405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050849
Samples
Known GenesUBTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144074
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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