A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378405



Internal ID21035958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16187689..16235652hg38UCSC Ensembl
chr5:16187798..16235761hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3847964
hg1947964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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