A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259907



Internal ID20469125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:84892592..84892592hg38UCSC Ensembl
chr2:85119716..85119716hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259907
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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