A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671038



Internal ID21619343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128912306..128912422hg38UCSC Ensembl
chrX:128046284..128046400hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165513
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671038
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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