A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201722



Internal ID20768763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180659611..180681760hg38UCSC Ensembl
chr1:180628747..180650896hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3822150
hg1922150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321987
Supporting Variants
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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