A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926812



Internal ID22702039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121848872..121849171hg38UCSC Ensembl
chr10:123608387..123608686hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361618
Samples
Known GenesATE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926812
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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