A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14350024



Internal ID22206945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22135242..22140263hg38UCSC Ensembl
chrX:22153359..22158380hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg385022
hg195022
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196479
Supporting Variants
SamplesHG00732
Known GenesPHEX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14350024
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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