A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165000



Internal ID21487001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102274524..102274578hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665828
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165000
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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