A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671909



Internal ID21620216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133635182..133635451hg38UCSC Ensembl
chrX:132769210..132769479hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165318
SamplesHG00513
Known GenesGPC3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671909
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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