A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611903



Internal ID21560208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30602817..30602817hg38UCSC Ensembl
chrX:30620934..30620934hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167002
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611903
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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