A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531666



Internal ID20905027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14246275..14257234hg38UCSC Ensembl
chr19:14357087..14368046hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3810960
hg1910960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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