A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373719



Internal ID21031272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57675291..57680106hg38UCSC Ensembl
chr3:57661018..57665833hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg384816
hg194816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102908
Samples
Known GenesDENND6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer