A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915502



Internal ID22690720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80205136..80227484hg38UCSC Ensembl
chr8:81117371..81139719hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3822349
hg1922349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915502
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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