A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405847



Internal ID21063400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:129129365..129204988hg38UCSC Ensembl
chr5:128465058..128540681hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3875624
hg1975624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124455
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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