A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4445487



Internal ID22111666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59406191..59406191hg38UCSC Ensembl
chr1:59871863..59871863hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765373
Samples
Known GenesFGGY
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4445487
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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