A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211292



Internal ID20778332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9857297..10031325hg38UCSC Ensembl
chr3:9898981..10073009hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38174029
hg19174029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366552
Supporting Variants
Samples
Known GenesCIDEC, CIDECP, CRELD1, EMC3, EMC3-AS1, FANCD2, IL17RC, IL17RE, JAGN1, LOC401052, PRRT3, PRRT3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211292
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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