A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003199



Internal ID21912542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141216434..141216494hg38UCSC Ensembl
chr7:140916234..140916294hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564416
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003199
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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