A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569748



Internal ID21761791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141411006..141411155hg38UCSC Ensembl
chr7:141110806..141110955hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012184
Supporting Variants
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569748
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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