A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378016



Internal ID21035569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103761049..103761461hg38UCSC Ensembl
chr4:104682206..104682618hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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