A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15759166



Internal ID22093638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139854666..139854666hg38UCSC Ensembl
chr4:140775820..140775820hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4443561
Supporting Variants
Samples
Known GenesMAML3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15759166
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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