A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165114



Internal ID21445103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120566369..120566369hg38UCSC Ensembl
chrX:119700224..119700224hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618585
Supporting Variants
SamplesHG00732
Known GenesCUL4B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165114
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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