A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166508



Internal ID21512134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152275152..152275207hg38UCSC Ensembl
chrX:151443624..151443679hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669971
Supporting Variants
SamplesNA24385
Known GenesGABRA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166508
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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