A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485879



Internal ID22543792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12462689..12467290hg38UCSC Ensembl
chr2:12602815..12607416hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg384602
hg194602
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485879
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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