A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4440768



Internal ID22106946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26242117..26242117hg38UCSC Ensembl
chr13:26816254..26816254hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15759280
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4440768
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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