A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165252



Internal ID21484520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110492977..110493029hg38UCSC Ensembl
chrX:109736205..109736257hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669621
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165252
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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