A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960282



Internal ID22735267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:52725050..52725050hg38UCSC Ensembl
chr4:53591217..53591217hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960282
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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