A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4444454



Internal ID22110634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120733293..120733293hg38UCSC Ensembl
chr10:122492805..122492805hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768095
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4444454
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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