A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477682



Internal ID21135235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61654153..61656607hg38UCSC Ensembl
chr14:62120871..62123325hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg382455
hg192455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020367
Samples
Known GenesFLJ22447
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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