A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442195



Internal ID22108378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158701140..158701140hg38UCSC Ensembl
chr6:159122172..159122172hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762341
Samples
Known GenesSYTL3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442195
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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