A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927067



Internal ID22702295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93282082..93286066hg38UCSC Ensembl
chr10:95041839..95045823hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383985
hg193985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927067
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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