A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165370



Internal ID21511634
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 StatusS
Merged Variantsnsv5669327
Supporting Variants
SamplesNA24385
Known GenesLDOC1, SPANXC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165370
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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