A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166317



Internal ID21461105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155387256..155453602hg38UCSC Ensembl
chrX:154616905..154683263hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3866347
hg1966359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670352
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166317
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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