A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094628



Internal ID20661668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158568733..158574705hg38UCSC Ensembl
chr3:158286522..158292494hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg385973
hg195973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368255
Supporting Variants
Samples
Known GenesLOC100996447, MLF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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