A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669327



Internal ID21617632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141114595..141472815hg38UCSC Ensembl
chrX:140208780..140560809hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38358221
hg19352030
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165370
SamplesNA24385
Known GenesLDOC1, SPANXC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669327
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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