A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359069



Internal ID21016622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97446401..97489800hg38UCSC Ensembl
chr3:97165245..97208644hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3843400
hg1943400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211273
Samples
Known GenesEPHA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359069
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