A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101884



Internal ID21291966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:13958994..13982942hg38UCSC Ensembl
InnerchrY:16070874..16094822hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3823949
hg1923949
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111276
Supporting Variants
Samplessample81
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101884
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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