A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950755



Internal ID22726151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:116764974..116764974hg38UCSC Ensembl
chr3:116483821..116483821hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950755
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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