A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220526



Internal ID20787566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101773536..102119723hg38UCSC Ensembl
chr7:101416816..101763003hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38346188
hg19346188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616669
Supporting Variants
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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