A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924623



Internal ID22699850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130350163..130405379hg38UCSC Ensembl
chr10:132148427..132203643hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3855217
hg1955217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924623
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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