A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953839



Internal ID21373908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6160960..6160960hg38UCSC Ensembl
chrX:6079001..6079001hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205525
SamplesHG002
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953839
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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