A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443012



Internal ID22109195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66036597..66036597hg38UCSC Ensembl
chrX:65256439..65256439hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15762439
Samples
Known GenesVSIG4
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443012
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