A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205728



Internal ID22354379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115403403..115403623hg38UCSC Ensembl
chrX:114637977..114638347hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38221
hg19371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353969, nssv14353970
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205728
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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