A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366817



Internal ID21024370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159782446..159784412hg38UCSC Ensembl
chr3:159500235..159502201hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg381967
hg191967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207976
Samples
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366817
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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