A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201674



Internal ID20768715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171219363..171224390hg38UCSC Ensembl
chr1:171188502..171193529hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg385028
hg195028
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329569
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201674
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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