A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489092



Internal ID21146645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87892496..87892970hg38UCSC Ensembl
chr13:88544751..88545225hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489092
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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