A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406074



Internal ID21063627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:91168146..91169739hg38UCSC Ensembl
chr5:90463963..90465556hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381594
hg191594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406074
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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