A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15757669



Internal ID22092086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:108689608..108689608hg38UCSC Ensembl
chr1:109232230..109232230hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444733
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15757669
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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