A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206779



Internal ID22355268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:137604960..137639734hg38UCSC Ensembl
OuterchrX:136687119..136721893hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3834775
hg1934775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14269828
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206779
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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