A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405027



Internal ID21062580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142388116..142389432hg38UCSC Ensembl
chr5:141767681..141768997hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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