A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858308



Internal ID22633243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148763098..148815191hg38UCSC Ensembl
chr7:148460190..148512283hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3852094
hg1952094
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17502619
Samples
Known GenesCUL1, EZH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858308
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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