A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366322



Internal ID21023875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155844073..155850827hg38UCSC Ensembl
chr3:155561862..155568616hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg386755
hg196755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096451
Samples
Known GenesSLC33A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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