A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4446437



Internal ID22112616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77279525..77279525hg38UCSC Ensembl
chr11:76990570..76990570hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763733
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4446437
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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