A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480920



Internal ID21138473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37760172..37793902hg38UCSC Ensembl
chr14:38229377..38263107hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3833731
hg1933731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480920
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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