A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4443103



Internal ID22109287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107910838..107910838hg38UCSC Ensembl
chrX:107154068..107154068hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15765554
Samples
Known GenesMID2
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4443103
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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