A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488891



Internal ID21146444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87169225..87259444hg38UCSC Ensembl
chr13:87821480..87911699hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3890220
hg1990220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014320
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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