A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359166



Internal ID21016719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23970151..23973543hg38UCSC Ensembl
chr4:23971774..23975166hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg383393
hg193393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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