A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366126



Internal ID21023679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67809067..68935602hg38UCSC Ensembl
chr3:67859491..68984753hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381126536
hg191125263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213007
Samples
Known GenesFAM19A1, FAM19A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366126
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