A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502085



Internal ID20875326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103026262..103026739hg38UCSC Ensembl
chr14:103492599..103493076hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015696
Samples
Known GenesCDC42BPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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