A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041602



Internal ID21950935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205255700..205255700hg38UCSC Ensembl
chr1:205224828..205224828hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527069
Samples
Known GenesTMCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041602
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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