A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16271925



Internal ID20481143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182741613..182741741hg38UCSC Ensembl
chr1:182710748..182710876hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738545
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16271925
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer