A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497288



Internal ID20870494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103214389..103215223hg38UCSC Ensembl
chr14:103680726..103681560hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38835
hg19835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015709
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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