A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444248



Internal ID22110428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125824766..125824766hg38UCSC Ensembl
chr10:127513335..127513335hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757534
Samples
Known GenesBCCIP
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444248
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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