A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761600



Internal ID22096098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133959980..133959980hg38UCSC Ensembl
chr8:134972223..134972223hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg381056
hg191056
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761600
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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