A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203477



Internal ID20770517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2652001..2683100hg38UCSC Ensembl
chr1:2583440..2614539hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3831100
hg1931100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325376
Supporting Variants
Samples
Known GenesTTC34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.47788


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