A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487808



Internal ID22545724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:152338570..152341247hg38UCSC Ensembl
chr2:153195084..153197761hg19UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg382678
hg192678
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831658
Supporting Variants
Samples
Known GenesFMNL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487808
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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