A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165535



Internal ID21471035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130989086..130989086hg38UCSC Ensembl
chrX:130123060..130123060hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614777
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165535
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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