A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376477



Internal ID21034030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148501801..148503400hg38UCSC Ensembl
chr4:149422953..149424552hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110226
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376477
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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