A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199137



Internal ID22348765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24258133..24258630hg38UCSC Ensembl
chrX:24276250..24276747hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350691
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199137
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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