A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953763



Internal ID22692991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150221810..150221810hg38UCSC Ensembl
chr3:149939597..149939597hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953763
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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