A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442369



Internal ID22108552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9388904..9388904hg38UCSC Ensembl
chrX:9356944..9356944hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766414
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442369
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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