A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670312



Internal ID21618619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:156021578..156022828hg38UCSC Ensembl
chrX:155251243..155252493hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166344
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670312
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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