A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937165



Internal ID21357234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:356823..356823hg38UCSC Ensembl
chrX:317558..317558hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205936
SamplesHG002
Known GenesPPP2R3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937165
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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