A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025667



Internal ID20592707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64426654..64429271hg38UCSC Ensembl
chr15:64718853..64721470hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382618
hg192618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507743
Supporting Variants
Samples
Known GenesTRIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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