A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405150



Internal ID21062703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143700420..143721217hg38UCSC Ensembl
chr5:143079985..143100782hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3820798
hg1920798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405150
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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