A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17494703



Internal ID22552635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70009729..70018851hg38UCSC Ensembl
chr3:70058880..70068002hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg389123
hg199123
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836745
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17494703
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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