A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599767



Internal ID21791814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25480199..25480324hg38UCSC Ensembl
chr13:26054337..26054462hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6035884
Supporting Variants
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599767
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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