A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205972



Internal ID22354586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:7053276..7076528hg38UCSC Ensembl
OuterchrY:6921317..6944569hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3823253
hg1923253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271170
SamplesNA19239
Known GenesTBL1Y
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205972
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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