A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209996



Internal ID20777036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52737861..52745068hg38UCSC Ensembl
chr3:52771877..52779084hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg387208
hg197208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360767
Supporting Variants
Samples
Known GenesNEK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209996
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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