A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5949267



Internal ID22724718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84850928..84850928hg38UCSC Ensembl
chr4:85772081..85772081hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411527
Samples
Known GenesWDFY3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5949267
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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