A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442868



Internal ID22109050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45721206..45721206hg38UCSC Ensembl
chrX:45580443..45580443hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763173
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442868
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