A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378837



Internal ID21036390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6205274..6206962hg38UCSC Ensembl
chr5:6205387..6207075hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg381689
hg191689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378837
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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