A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356615



Internal ID21014168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6226995..6229762hg38UCSC Ensembl
chr4:6228722..6231489hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg382768
hg192768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118521
Samples
Known GenesLOC285484
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356615
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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