A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566983



Internal ID21515314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68197896..68200783hg38UCSC Ensembl
chr4:69063614..69066501hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382888
hg192888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134236
SamplesHG00731
Known GenesFTLP10, TMPRSS11BNL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566983
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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