A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476206



Internal ID21133759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:41244361..41376908hg38UCSC Ensembl
chr14:41713564..41846111hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38132548
hg19132548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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