A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926841



Internal ID22702069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35872417..35875750hg38UCSC Ensembl
chr10:36161345..36164678hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg383334
hg193334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926841
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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