A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497527



Internal ID22555461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98392723..98404986hg38UCSC Ensembl
chr3:98111567..98123830hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3812264
hg1912264
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836925
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497527
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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