A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516940



Internal ID20890301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51216244..51230299hg38UCSC Ensembl
chr19:51719500..51733555hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3814056
hg1914056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048709
Samples
Known GenesCD33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516940
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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