A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386079



Internal ID21043632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103789742..103790226hg38UCSC Ensembl
chr4:104710899..104711383hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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