A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562136



Internal ID335095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85027633..85027684hg38UCSC Ensembl
chrX:84282639..84282690hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741166
Samples
Known GenesAPOOL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562136
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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