A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480558



Internal ID22538461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158790317..158831078hg38UCSC Ensembl
chr2:159646829..159687590hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3840762
hg1940762
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831379
Supporting Variants
Samples
Known GenesDAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480558
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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