A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191198



Internal ID22341937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:35418022..35437453hg38UCSC Ensembl
OuterchrX:35436139..35455570hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3819432
hg1919432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14268958
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191198
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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