A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573343



Internal ID21765386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137459477..137459477hg38UCSC Ensembl
chr7:137144223..137144223hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077081
Supporting Variants
Samples
Known GenesDGKI
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573343
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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