A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202847



Internal ID20769887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25989649..25991263hg38UCSC Ensembl
chr1:26316140..26317754hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381615
hg191615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328988
Supporting Variants
Samples
Known GenesPAFAH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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