A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444269



Internal ID22110449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63546499..63546499hg38UCSC Ensembl
chr20:62177852..62177852hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765598
Samples
Known GenesSRMS
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444269
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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