A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613330



Internal ID20986401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144029926..144043760hg38UCSC Ensembl
chr6:144351063..144364897hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3813835
hg1913835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140260
Samples
Known GenesPLAGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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