A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4447598



Internal ID22113775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66431848..66431848hg38UCSC Ensembl
chr2:66658980..66658980hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15768270
Samples
Known GenesMEIS1-AS3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4447598
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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