A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3932909



Internal ID21352978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151743041..151743041hg38UCSC Ensembl
chrX:150911513..150911513hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205774
SamplesHG002
Known GenesCNGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3932909
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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