A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535252



Internal ID21859607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:212981973..212982058hg38UCSC Ensembl
chr2:213846697..213846782hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987392
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535252
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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