A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665183



Internal ID21613488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39050656..39050736hg38UCSC Ensembl
chrX:38909909..38909989hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167369
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665183
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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