A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911502



Internal ID22686716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69853528..69853613hg38UCSC Ensembl
chr10:71613284..71613369hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359670
Samples
Known GenesCOL13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911502
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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