A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442205



Internal ID22108388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122902326..122902326hg38UCSC Ensembl
chr12:123386873..123386873hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763393
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442205
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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