A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102263



Internal ID21279578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21021832..21047615hg38UCSC Ensembl
InnerchrY:23183718..23209501hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3825784
hg1925784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114060
Supporting Variants
Samplessample286
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102263
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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