A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375413



Internal ID21032966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17955935..17956403hg38UCSC Ensembl
chr4:17957558..17958026hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115052
Samples
Known GenesLCORL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375413
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