A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389606



Internal ID21047159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169755078..169784976hg38UCSC Ensembl
chr4:170676229..170706127hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3829899
hg1929899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115712
Samples
Known GenesC4orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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