A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167512



Internal ID21509092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5559176..5559176hg38UCSC Ensembl
chrX:5477217..5477217hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3825720
hg1925720
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614139
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167512
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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