A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166658



Internal ID21461214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:224663..224663hg38UCSC Ensembl
chrY:12266..12266hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618860
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166658
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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