A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102247



Internal ID21276364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:3249400..3295612hg38UCSC Ensembl
InnerchrY:3117441..3163653hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3846213
hg1946213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110858
Supporting Variants
Samplessample235
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102247
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer