A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413185



Internal ID21070738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126850885..126908109hg38UCSC Ensembl
chr5:126186577..126243801hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3857225
hg1957225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213188
Samples
Known GenesMARCH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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