A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482758



Internal ID21140311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74063201..74063900hg38UCSC Ensembl
chr14:74529904..74530603hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021446
Samples
Known GenesALDH6A1, CCDC176
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482758
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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