A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111552



Internal ID21294818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:15823009..15894312hg38UCSC Ensembl
InnerchrY:17934889..18006192hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3871304
hg1971304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102264
Samplessample287
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111552
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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