A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495512



Internal ID21153065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35233086..35233672hg38UCSC Ensembl
chr14:35702292..35702878hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18017272
Samples
Known GenesKIAA0391
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495512
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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