A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609460



Internal ID21557765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13675492..13675492hg38UCSC Ensembl
chrX:13693611..13693611hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165713
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609460
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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