A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442984



Internal ID22109167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101137985..101137985hg38UCSC Ensembl
chrX:100392974..100392974hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15757585
Samples
Known GenesCENPI
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442984
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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