A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619058



Internal ID21567363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6160960..6160960hg38UCSC Ensembl
chrX:6079001..6079001hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167691
SamplesHG00731
Known GenesNLGN4X
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619058
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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