A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209761



Internal ID20776802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:156808501..156832000hg38UCSC Ensembl
chr3:156526290..156549789hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3823500
hg1923500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365191
Supporting Variants
Samples
Known GenesLEKR1, LINC00886, PA2G4P4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209761
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00071


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