A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490115



Internal ID21147668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69212107..69216705hg38UCSC Ensembl
chr14:69678824..69683422hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg384599
hg194599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020587
Samples
Known GenesEXD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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