A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210019



Internal ID20777059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5410107..8236984hg38UCSC Ensembl
chr3:5451793..8278671hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382826878
hg192826879
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368580
Supporting Variants
Samples
Known GenesGRM7, LMCD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210019
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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