A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761813



Internal ID22096311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127666470..127666470hg38UCSC Ensembl
chr2:128424044..128424044hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4448489
Supporting Variants
Samples
Known GenesLIMS2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761813
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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