A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366552



Internal ID21024105
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 StatusM
Merged Variants
Supporting Variantsnssv18211292
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)nsv6366552
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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