A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201068



Internal ID20768108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175299241..175338809hg38UCSC Ensembl
chr1:175268377..175307945hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3839569
hg1939569
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335371
Supporting Variants
Samples
Known GenesTNR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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