A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922046



Internal ID22697271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:56789858..56825705hg38UCSC Ensembl
chr10:58549618..58585465hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3835848
hg1935848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922046
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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