A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670131



Internal ID21618438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40862585..40863069hg38UCSC Ensembl
chrX:40721838..40722322hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167094
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670131
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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