A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526994



Internal ID20900355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16025475..16028162hg38UCSC Ensembl
chr19:16136285..16138972hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382688
hg192688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044460
Samples
Known GenesLINC00661
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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