A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102264



Internal ID21279657
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 StatusS
Merged Variantsnsv3111552
Supporting Variants
Samplessample287
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102264
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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