A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368056



Internal ID21025609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97655639..97663846hg38UCSC Ensembl
chr3:97374483..97382690hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg388208
hg198208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211276
Samples
Known GenesEPHA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368056
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