A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011116



Internal ID21920459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155305670..155305724hg38UCSC Ensembl
chr6:155626804..155626858hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563198
Samples
Known GenesTFB1M
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011116
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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