A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17529218



Internal ID21853575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:108468855..108468855hg38UCSC Ensembl
chr2:109085311..109085311hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048809
Supporting Variants
Samples
Known GenesGCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17529218
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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