A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437658



Internal ID22103838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3031218..3031218hg38UCSC Ensembl
chr17:2934512..2934512hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761944
Samples
Known GenesRAP1GAP2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437658
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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