A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497512



Internal ID22555446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97771571..97780106hg38UCSC Ensembl
chr3:97490415..97498950hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg388536
hg198536
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837479
Supporting Variants
Samples
Known GenesARL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497512
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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