A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665564



Internal ID21613869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154402438..154402633hg38UCSC Ensembl
chrX:153630779..153630974hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166285
SamplesNA19650
Known GenesDNASE1L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665564
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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