A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403867



Internal ID21061420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:72660371..72745965hg38UCSC Ensembl
chr5:71956198..72041792hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3885595
hg1985595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216303
Samples
Known GenesLOC102477328
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403867
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer