A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406587



Internal ID21064140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:144498128..144515355hg38UCSC Ensembl
chr5:143877691..143894918hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3817228
hg1917228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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