A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437896



Internal ID22104076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17252404..17252404hg38UCSC Ensembl
chr17:17155718..17155718hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767942
Samples
Known GenesCOPS3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437896
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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