A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15206032



Internal ID21344830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80215125..80215125hg38UCSC Ensembl
chrX:79470624..79470624hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3949544
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15206032
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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