A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665890



Internal ID21614195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18262540..18262926hg38UCSC Ensembl
chrX:18280660..18281046hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166548
SamplesNA19238
Known GenesSCML2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665890
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer