A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166073



Internal ID21470942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151016643..151016643hg38UCSC Ensembl
chrX:150185116..150185116hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622657
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166073
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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