A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390576



Internal ID21048129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168602522..168607856hg38UCSC Ensembl
chr4:169523673..169529007hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385335
hg195335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115356
Samples
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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