A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406789



Internal ID21064342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:101606505..101915615hg38UCSC Ensembl
chr5:100942209..101251319hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38309111
hg19309111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5846n223
Supporting Variantsnssv18122264
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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