A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389343



Internal ID21046896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10835549..10840652hg38UCSC Ensembl
chr5:10835661..10840764hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385104
hg195104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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