A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485506



Internal ID22543417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42831848..42833777hg38UCSC Ensembl
chr2:43058988..43060917hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381930
hg191930
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5833011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485506
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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