A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6075072



Internal ID21984305
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 StatusM
Merged Variants
Supporting Variantsnssv17561226
Samples
Known GenesTBXAS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6075072
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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