A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191841



Internal ID22342495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142351552..142351618hg38UCSC Ensembl
chrX:141439338..141439404hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353347, nssv14353348
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191841
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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