A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205255



Internal ID21344057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101137985..101137985hg38UCSC Ensembl
chrX:100392974..100392974hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937959
Supporting Variants
SamplesHG002
Known GenesCENPI
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205255
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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