A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399299



Internal ID21056852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77851801..77852100hg38UCSC Ensembl
chr5:77147625..77147924hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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