A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4442866



Internal ID22109048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45121761..45121761hg38UCSC Ensembl
chrX:44981006..44981006hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15766804
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4442866
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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