A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907513



Internal ID22682722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96819229..96834065hg38UCSC Ensembl
chr4:97740380..97755216hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3814837
hg1914837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416921
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907513
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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