A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437088



Internal ID22103265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220523716..220523716hg38UCSC Ensembl
chr2:221388437..221388437hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756602
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437088
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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