A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210011



Internal ID20777051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53207276..53208357hg38UCSC Ensembl
chr3:53241292..53242373hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210011
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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