A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17524811



Internal ID21849169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88127043..88127043hg38UCSC Ensembl
chr2:88426562..88426562hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045971
Supporting Variants
Samples
Known GenesFABP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17524811
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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