A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165118



Internal ID21509397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120687966..120687966hg38UCSC Ensembl
chrX:119821821..119821821hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614085
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165118
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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