A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404362



Internal ID22462232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127246262..127246262hg38UCSC Ensembl
chr3:126965105..126965105hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948456
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404362
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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