A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166011



Internal ID21457340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136125250..136125315hg38UCSC Ensembl
chrX:135207409..135207474hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669572
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166011
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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