A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484891



Internal ID22542801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102315036..102320550hg38UCSC Ensembl
chr2:102931496..102937010hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg385515
hg195515
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831151
Supporting Variants
Samples
Known GenesIL1RL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484891
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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