A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508271



Internal ID20881570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:92870601..92872400hg38UCSC Ensembl
chr14:93336946..93338745hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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