A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4449492



Internal ID22115669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77036103..77036103hg38UCSC Ensembl
chr8:77948339..77948339hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15767380
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4449492
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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