A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762781



Internal ID22097267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158566405..158566405hg38UCSC Ensembl
chr6:158987437..158987437hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4442193
Supporting Variants
Samples
Known GenesTMEM181
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762781
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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