A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17483693



Internal ID22541600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109165072..109199615hg38UCSC Ensembl
chr3:108883919..108918462hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3834544
hg1934544
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834261
Supporting Variants
Samples
Known GenesLINC00488
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17483693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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