A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516708



Internal ID20890069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28552105..28582508hg38UCSC Ensembl
chr19:29043012..29073415hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3830404
hg1930404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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