A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932715



Internal ID22708018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69884926..69885239hg38UCSC Ensembl
chr13:70459058..70459371hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388401
Samples
Known GenesKLHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932715
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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