A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489307



Internal ID21146860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95371071..95382388hg38UCSC Ensembl
chr13:96023325..96034642hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3811318
hg1911318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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