A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575354



Internal ID21523783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67634003..67641447hg38UCSC Ensembl
chr8:68546238..68553682hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg387445
hg197445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157223
SamplesHG02587
Known GenesCPA6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575354
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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