A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840103



Internal ID22615038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71646834..71650482hg38UCSC Ensembl
chr4:72512551..72516199hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg383649
hg193649
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840103
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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