A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203471



Internal ID20770511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26325493..26390806hg38UCSC Ensembl
chr1:26651984..26717297hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3865314
hg1965314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331344
Supporting Variants
Samples
Known GenesAIM1L, ZNF683
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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