A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073194



Internal ID21982427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170318566..170318566hg38UCSC Ensembl
chr6:170627654..170627654hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570356
Samples
Known GenesFAM120B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073194
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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