A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622210



Internal ID21570515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15608728..15608728hg38UCSC Ensembl
chrX:15626851..15626851hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166353
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622210
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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