A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201833



Internal ID20768874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202837701..202839234hg38UCSC Ensembl
chr1:202806829..202808362hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381534
hg191534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321798
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201833
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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