A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483444



Internal ID21140997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:87816787..87817724hg38UCSC Ensembl
chr14:88283131..88284068hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38938
hg19938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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