A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379304



Internal ID21036857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94599841..94600534hg38UCSC Ensembl
chr4:95520992..95521685hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120777
Samples
Known GenesPDLIM5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379304
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