A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389656



Internal ID21047209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94306871..94309611hg38UCSC Ensembl
chr4:95228022..95230762hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg382741
hg192741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120554
Samples
Known GenesHPGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389656
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