A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206138



Internal ID22354725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:4642902..4653065hg38UCSC Ensembl
OuterchrY:4510943..4521106hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3810164
hg1910164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271191
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206138
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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