A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211524



Internal ID20778564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180647475..180665941hg38UCSC Ensembl
chr3:180365263..180383729hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3818467
hg1918467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365364
Supporting Variants
Samples
Known GenesCCDC39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211524
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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