A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168160



Internal ID21480431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70372084..70372084hg38UCSC Ensembl
chrX:69591934..69591934hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615311
Supporting Variants
SamplesHG03683
Known GenesKIF4A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168160
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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