A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576026



Internal ID21768069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73428024..73428024hg38UCSC Ensembl
chr7:72842354..72842354hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576026
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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