A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437783



Internal ID22103963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234514581..234514581hg38UCSC Ensembl
chr2:235423225..235423225hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38959
hg19959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761311
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437783
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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