A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668947



Internal ID21617252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125321662..125321724hg38UCSC Ensembl
chrX:124455511..124455573hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165600
SamplesNA19238
Known GenesLOC100129520
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668947
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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