A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16294860



Internal ID20504078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11330719..11330719hg38UCSC Ensembl
chr2:11470845..11470845hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751242
Supporting Variants
Samples
Known GenesROCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16294860
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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