A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17523064



Internal ID21847423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11636916..11636916hg38UCSC Ensembl
chr2:11777042..11777042hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051317
Supporting Variants
Samples
Known GenesGREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17523064
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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