A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15206059



Internal ID21344727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110705431..110705431hg38UCSC Ensembl
chrX:109948659..109948659hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949591
Supporting Variants
SamplesHG002
Known GenesCHRDL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15206059
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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