A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365415



Internal ID21022968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14119422..14119496hg38UCSC Ensembl
chr3:14160922..14160996hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094292
Samples
Known GenesCHCHD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365415
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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