A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379556



Internal ID21037109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145107250..145107445hg38UCSC Ensembl
chr4:146028402..146028597hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18108858
Samples
Known GenesABCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379556
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