A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516612



Internal ID20889973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18786812..18802173hg38UCSC Ensembl
chr19:18897621..18912982hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3815362
hg1915362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045121
Samples
Known GenesCOMP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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