A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207787



Internal ID22356127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94145915..94149721hg38UCSC Ensembl
chrX:93400914..93404720hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg383807
hg193807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14353039
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207787
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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