A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504066



Internal ID20877325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97403792..97404168hg38UCSC Ensembl
chr14:97870129..97870505hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022500
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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