A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515614



Internal ID20888975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19666120..19680030hg38UCSC Ensembl
chr19:19776929..19790839hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3813911
hg1913911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045444
Samples
Known GenesZNF101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515614
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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