A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211248



Internal ID20778288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95758740..95790551hg38UCSC Ensembl
chr3:95477584..95509395hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3831812
hg1931812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363816
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211248
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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