A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488281



Internal ID22546198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162174047..162184073hg38UCSC Ensembl
chr2:163030557..163040583hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3810027
hg1910027
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831404
Supporting Variants
Samples
Known GenesFAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488281
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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