A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4439601



Internal ID22105779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101680713..101680713hg38UCSC Ensembl
chr3:101399557..101399557hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15758888
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4439601
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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