A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4436937



Internal ID22103114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102631765..102631765hg38UCSC Ensembl
chr8:103643993..103643993hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765182
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4436937
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer