A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605679



Internal ID21553984
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 StatusM
Merged Variants
Supporting Variantsnssv17168544
SamplesHG00864
Known GenesKLHL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605679
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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