A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442841



Internal ID22109023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80193740..80193740hg38UCSC Ensembl
chrX:79449239..79449239hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15756520
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442841
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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