A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611822



Internal ID21560127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130148900..130148900hg38UCSC Ensembl
chrX:129282875..129282875hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165521
SamplesNA19238
Known GenesAIFM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611822
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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