A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862807



Internal ID22637742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157155845..157157711hg38UCSC Ensembl
chr7:156948539..156950405hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381867
hg191867
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17504651
Samples
Known GenesUBE3C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862807
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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