A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484873



Internal ID22542783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100278080..100281717hg38UCSC Ensembl
chr2:100894542..100898179hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg383638
hg193638
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830866
Supporting Variants
Samples
Known GenesLONRF2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484873
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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