A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670238



Internal ID21618545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121172376..121172472hg38UCSC Ensembl
chrX:120306230..120306326hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165127
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670238
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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