A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192119



Internal ID22342744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:33792411..33842944hg38UCSC Ensembl
OuterchrX:33810528..33861061hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3850534
hg1950534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14268957
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192119
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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