A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16264069



Internal ID20473287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141410999..141410999hg38UCSC Ensembl
chr7:141110799..141110799hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756493
Supporting Variants
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16264069
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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