A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914586



Internal ID22689803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127594059..127594280hg38UCSC Ensembl
chr7:127234113..127234334hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447338
Samples
Known GenesFSCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914586
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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