A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416933



Internal ID22474803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99605795..99611786hg38UCSC Ensembl
chr3:99324639..99330630hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg385992
hg195992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890436
Supporting Variants
Samples
Known GenesMIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416933
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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