A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192515



Internal ID22343091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45836197..45836504hg38UCSC Ensembl
chrX:45695624..45695929hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38308
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351092
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192515
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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