A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168945



Internal ID21447174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:89484727..89484727hg38UCSC Ensembl
chrX:88739726..88739726hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611416
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168945
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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