A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518865



Internal ID20892226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45133373..45136030hg38UCSC Ensembl
chr19:45636631..45639288hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048635
Samples
Known GenesPPP1R37
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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