A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390132



Internal ID21047685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:37901890..37902356hg38UCSC Ensembl
chr5:37901992..37902458hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38467
hg19467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390132
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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