A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358983



Internal ID21016536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9923511..9929275hg38UCSC Ensembl
chr3:9965195..9970959hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg385765
hg195765
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211304
Samples
Known GenesIL17RC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358983
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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