A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490426



Internal ID21147979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73616602..73619037hg38UCSC Ensembl
chr14:74083306..74085741hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382436
hg192436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020180
Samples
Known GenesACOT6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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