A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960087



Internal ID22722168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181377161..181377161hg38UCSC Ensembl
chr4:182298314..182298314hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960087
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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