A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615668



Internal ID21563973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120784977..120784977hg38UCSC Ensembl
chrX:119918831..119918831hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165121
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615668
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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