A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272508



Internal ID20481726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51861124..51861124hg38UCSC Ensembl
chr7:51928820..51928820hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272508
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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