A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950139



Internal ID21370208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112709927..112709927hg38UCSC Ensembl
chrX:111953155..111953155hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38921
hg19921
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15206067
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950139
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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