A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906025



Internal ID22681219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116254396..116290766hg38UCSC Ensembl
chr5:115590093..115626463hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3836371
hg1936371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425594
Samples
Known GenesCOMMD10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906025
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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