A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201848



Internal ID20768889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203946259..203983619hg38UCSC Ensembl
chr1:203915387..203952747hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3837361
hg1937361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201848
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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