A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211278



Internal ID20778318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97844357..97999939hg38UCSC Ensembl
chr3:97563201..97718783hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38155583
hg19155583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363280
Supporting Variants
Samples
Known GenesCRYBG3, GABRR3, MINA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211278
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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