A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406999



Internal ID21064552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98032096..98105318hg38UCSC Ensembl
chr5:97367800..97441022hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3873223
hg1973223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136535
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406999
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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