A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165191



Internal ID21457322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104347660..104347660hg38UCSC Ensembl
chrX:103592341..103592341hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611383
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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