A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606589



Internal ID21554894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104250409..104250409hg38UCSC Ensembl
chrX:103495090..103495090hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165190
SamplesHG03486
Known GenesESX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606589
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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