A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167427



Internal ID21473623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49184141..49184141hg38UCSC Ensembl
chrX:49040594..49040594hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623051
Supporting Variants
SamplesHG03371
Known GenesPRICKLE3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167427
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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