A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168544



Internal ID21448611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87663423..87663423hg38UCSC Ensembl
chrX:86918423..86918423hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605679
Supporting Variants
SamplesHG00864
Known GenesKLHL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168544
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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