A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035884



Internal ID21945227
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 StatusM
Merged Variants
Supporting Variantsnssv17599767
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035884
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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