A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17487476



Internal ID22545392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57908902..57914859hg38UCSC Ensembl
chr2:58136037..58141994hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg385958
hg195958
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833068
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17487476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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