A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413506



Internal ID21071059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139483140..139485321hg38UCSC Ensembl
chr5:138862725..138864906hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg382182
hg192182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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