A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166333



Internal ID21430061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155708210..156030894hg38UCSC Ensembl
chrX:154937871..155260559hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38322685
hg19322689
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665408
Supporting Variants
SamplesHG00731
Known GenesIL9R, SPRY3, VAMP7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166333
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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