A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5964326



Internal ID22739261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174408027..174408027hg38UCSC Ensembl
chr4:175329178..175329178hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17423665
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5964326
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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