A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225153



Internal ID22368369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:17946180..17954083hg38UCSC Ensembl
OuterchrY:20058060..20065963hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271213
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225153
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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