A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192106



Internal ID22342734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23850382..23850442hg38UCSC Ensembl
chrX:23868499..23868559hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350678, nssv14350677
SamplesHG00512, HG00514
Known GenesAPOO
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192106
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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