A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761598



Internal ID22096096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124482952..124482952hg38UCSC Ensembl
chr8:125495193..125495193hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4437094
Supporting Variants
Samples
Known GenesRNF139
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761598
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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