A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490912



Internal ID21148465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:38669516..38817066hg38UCSC Ensembl
chr14:39138720..39286270hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38147551
hg19147551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018169
Samples
Known GenesLINC00639
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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