A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484896



Internal ID22542806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10293374..10298902hg38UCSC Ensembl
chr2:10433500..10439028hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg385529
hg195529
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831062
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484896
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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