A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488087



Internal ID21145640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:42927054..43043627hg38UCSC Ensembl
chr14:43396257..43512830hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38116574
hg19116574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018292
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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