A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513363



Internal ID20886707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:103631322..103645925hg38UCSC Ensembl
chr14:104097659..104112262hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3814604
hg1914604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015933
Samples
Known GenesKLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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