A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167017



Internal ID21492652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30788651..30804883hg38UCSC Ensembl
chrX:30806768..30823000hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3816233
hg1916233
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666405
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167017
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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