A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17561226



Internal ID21885581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139950802..139950802hg38UCSC Ensembl
chr7:139650601..139650601hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6075072
Supporting Variants
Samples
Known GenesTBXAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17561226
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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