A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666162



Internal ID21614467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30329648..30330479hg38UCSC Ensembl
chrX:30347765..30348596hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38832
hg19832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166984
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666162
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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