A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955238



Internal ID22730452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42883933..42883933hg38UCSC Ensembl
chr7:42923532..42923532hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955238
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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