A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449280



Internal ID22115457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:166889878..166889878hg38UCSC Ensembl
chr2:167746388..167746388hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg383210
hg193210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767570
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449280
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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