A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484768



Internal ID22542677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3604220..3606119hg38UCSC Ensembl
chr2:3651810..3653709hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832970
Supporting Variants
Samples
Known GenesCOLEC11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484768
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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