A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411162



Internal ID21068715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153828223..153833220hg38UCSC Ensembl
chr5:153207783..153212780hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg384998
hg194998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126782
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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