A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399996



Internal ID21057549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:100065175..100379308hg38UCSC Ensembl
chr5:99400879..99715012hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38314134
hg19314134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5840n223
Supporting Variantsnssv18123261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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