A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537149



Internal ID21861504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:181124517..181124517hg38UCSC Ensembl
chr1:181093653..181093653hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045492
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537149
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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