A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409531



Internal ID21067084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166410701..166422900hg38UCSC Ensembl
chr5:165837706..165849905hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3812200
hg1912200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6019n223
Supporting Variantsnssv18127382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409531
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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