A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610182



Internal ID21558487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121788421..121788421hg38UCSC Ensembl
chrX:120922274..120922274hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165137
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610182
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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