A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203470



Internal ID20770510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26310499..26312940hg38UCSC Ensembl
chr1:26636990..26639431hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382442
hg192442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324830
Supporting Variants
Samples
Known GenesUBXN11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203470
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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