A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369507



Internal ID21027060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4494040..4508903hg38UCSC Ensembl
chr4:4495767..4510630hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3814864
hg1914864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18117596
Samples
Known GenesSTX18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369507
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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