A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532587



Internal ID20905948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4601780..4649655hg38UCSC Ensembl
chr19:4601792..4649667hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3847876
hg1947876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046553
Samples
Known GenesTNFAIP8L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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