A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166111



Internal ID21492832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153481271..153481322hg38UCSC Ensembl
chrX:152746729..152746780hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665133
Supporting Variants
SamplesNA19238
Known GenesHAUS7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166111
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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