A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395839



Internal ID21053392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61324862..61327148hg38UCSC Ensembl
chr5:60620689..60622975hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg382287
hg192287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395839
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