A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575322



Internal ID21523750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158704814..158705275hg38UCSC Ensembl
chr6:159125846..159126307hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17147590
SamplesHG00512
Known GenesSYTL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575322
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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