A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940574



Internal ID22715985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25977173..25977329hg38UCSC Ensembl
chr13:26551311..26551467hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369852
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940574
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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