A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15756191



Internal ID22090675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119525206..119525206hg38UCSC Ensembl
chr2:120282782..120282782hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4448127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15756191
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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