A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102300



Internal ID21286809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:12287023..12292262hg38UCSC Ensembl
InnerchrY:14407725..14412965hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg385240
hg195241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117942
Supporting Variants
Samplessample394
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102300
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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