A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192239



Internal ID22342851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9795815..9817089hg38UCSC Ensembl
OuterchrY:9633424..9654698hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3821275
hg1921275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271176
SamplesNA19239
Known GenesTTTY22
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192239
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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