A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142865



Internal ID20709905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33797524..33802607hg38UCSC Ensembl
chr6:33765301..33770384hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg385084
hg195084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403718
Supporting Variants
Samples
Known GenesMLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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