A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569702



Internal ID21518063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158704814..158704864hg38UCSC Ensembl
chr6:159125846..159125896hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158277
SamplesHG00731
Known GenesSYTL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569702
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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