A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439288



Internal ID22105465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:125307743..125307743hg38UCSC Ensembl
chr12:125792289..125792289hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758760
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439288
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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