A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558062



Internal ID21882417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23507864..23507864hg38UCSC Ensembl
chr7:23547483..23547483hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6069454
Supporting Variants
Samples
Known GenesTRA2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558062
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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