A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505221



Internal ID20878487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103677854..103679153hg38UCSC Ensembl
chr14:104144191..104145490hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015938
Samples
Known GenesKLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505221
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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