A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166758



Internal ID21451250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2841710..2841710hg38UCSC Ensembl
chrX:2759751..2759751hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624509
Supporting Variants
SamplesHG01505
Known GenesGYG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166758
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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