A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406170



Internal ID21063723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149476569..149480567hg38UCSC Ensembl
chr5:148856132..148860130hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg383999
hg193999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18128001
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406170
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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