A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624305



Internal ID21572610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:12924466..12924466hg38UCSC Ensembl
chrX:12942585..12942585hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165660
SamplesNA19238
Known GenesTLR8-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624305
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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