A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486829



Internal ID21144382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69431155..69434200hg38UCSC Ensembl
chr14:69897872..69900917hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg383046
hg193046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020595
Samples
Known GenesSLC39A9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486829
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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