A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910546



Internal ID22685757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29757482..29760946hg38UCSC Ensembl
chr8:29614998..29618462hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383465
hg193465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435401
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910546
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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