A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442490



Internal ID22108673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30310880..30310880hg38UCSC Ensembl
chrX:30328997..30328997hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15763172
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442490
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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