A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567439



Internal ID21515775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155305488..155305559hg38UCSC Ensembl
chr6:155626622..155626693hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143925
SamplesHG01596
Known GenesTFB1M
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567439
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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