A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408240



Internal ID21065793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162183069..162214526hg38UCSC Ensembl
chr5:161610075..161641532hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3831458
hg1931458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6009n223
Supporting Variantsnssv18126677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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