A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536971



Internal ID312356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:12924468..12924517hg38UCSC Ensembl
chrX:12942587..12942636hg19UCSC 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 Variantsnssv17739299
Samples
Known GenesTLR8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536971
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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