A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380428



Internal ID21037981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41162024..41162614hg38UCSC Ensembl
chr5:41162126..41162716hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131546
Samples
Known GenesC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380428
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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