A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529065



Internal ID20902426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37956704..37962364hg38UCSC Ensembl
chr19:38447344..38453004hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg385661
hg195661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198093
Samples
Known GenesSIPA1L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529065
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