A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531925



Internal ID21856281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3591573..3591573hg38UCSC Ensembl
chr2:3639163..3639163hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042433
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531925
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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