A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095169



Internal ID20662209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12161492..12163344hg38UCSC Ensembl
chr3:12202992..12204844hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg381853
hg191853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365403
Supporting Variants
Samples
Known GenesSYN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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