A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530701



Internal ID21855057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27914870..27914870hg38UCSC Ensembl
chr2:28137737..28137737hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043258
Supporting Variants
Samples
Known GenesBRE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530701
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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