A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438819



Internal ID22104996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51729913..51729913hg38UCSC Ensembl
chr3:51763929..51763929hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767991
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4438819
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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