A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929782



Internal ID22705041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102620866..102620955hg38UCSC Ensembl
chr12:103014644..103014733hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929782
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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