A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3248396



Internal ID22376975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103754225..103761646hg38UCSC Ensembl
chrX:103009153..103016574hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg387422
hg197422
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353155, nssv14353154
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3248396
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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