A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18091227



Internal ID20658267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102988914..102990712hg38UCSC Ensembl
chr3:102707758..102709556hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg381799
hg191799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18091227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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