A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5569845



Internal ID21518207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39374555..39529708hg38UCSC Ensembl
chr8:39232074..39387227hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38155154
hg19155154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158437
SamplesHG00096
Known GenesADAM3A, ADAM5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5569845
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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