A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415573



Internal ID21073126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90257992..90295349hg38UCSC Ensembl
chr5:89553809..89591166hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3837358
hg1937358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214993
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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