A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202747



Internal ID20769787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229333106..229333764hg38UCSC Ensembl
chr1:229468853..229469511hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38659
hg19659
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334429
Supporting Variants
Samples
Known GenesCCSAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202747
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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