A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203544



Internal ID20770584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28582847..28586504hg38UCSC Ensembl
chr1:28909359..28913016hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383658
hg193658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329724
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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