A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874701



Internal ID22649654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9602253..9743885hg38UCSC Ensembl
chrX:9570293..9711925hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38141633
hg19141633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455600
Samples
Known GenesGPR143, TBL1X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874701
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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