A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668859



Internal ID21617164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:114261281..114261344hg38UCSC Ensembl
chrX:113504500..113504595hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3864
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165033
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668859
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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