A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925338



Internal ID22700565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59426838..59427990hg38UCSC Ensembl
chr10:61186596..61187748hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925338
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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