A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102252



Internal ID21277155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:15110826..15631616hg38UCSC Ensembl
InnerchrY:17222706..17743496hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38520791
hg19520791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116277
Supporting Variants
Samplessample246
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102252
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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