A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492882



Internal ID21150435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:39662939..39809070hg38UCSC Ensembl
chr14:40132143..40278274hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38146132
hg19146132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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