A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4437749



Internal ID22103929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6438313..6438313hg38UCSC Ensembl
chr17:6341633..6341633hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15761950
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4437749
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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