A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383442



Internal ID21040995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6517764..6519474hg38UCSC Ensembl
chr5:6517877..6519587hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg381711
hg191711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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