A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925864



Internal ID22701091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119635809..119638562hg38UCSC Ensembl
chr10:121395321..121398074hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382754
hg192754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925864
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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