A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007429



Internal ID20574469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112866640..112919380hg38UCSC Ensembl
chr13:113520954..113573694hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3852741
hg1952741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480210
Supporting Variants
Samples
Known GenesATP11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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