A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190795



Internal ID22341604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41262127..41262244hg38UCSC Ensembl
chrX:41121380..41121497hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350372
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190795
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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