A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953066



Internal ID22728362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155017347..155017347hg38UCSC Ensembl
chr1:154989823..154989823hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368959
Samples
Known GenesZBTB7B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953066
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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